Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation

Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Saji Philip [verfasserIn] Sarasa Bharati [verfasserIn] Kottureth Mammen Cherian [verfasserIn] Saroja Bharati [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2016

Schlagwörter:	dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly

Übergeordnetes Werk:	In: American Journal of Perinatology Reports - Thieme Medical Publishers, Inc., 2014, 06(2016), 01, Seite e91-e95
Übergeordnetes Werk:	volume:06 ; year:2016 ; number:01 ; pages:e91-e95

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.1055/s-0035-1566296

Katalog-ID:	DOAJ074821601

Internformat


LEADER	01000caa a22002652 4500
001	DOAJ074821601
003	DE-627
005	20230309130600.0
007	cr uuu---uuuuu
008	230228s2016 xx \|\|\|\|\|o 00\| \|\|eng c
024	7		\|a 10.1055/s-0035-1566296 \|2 doi
035			\|a (DE-627)DOAJ074821601
035			\|a (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02
040			\|a DE-627 \|b ger \|c DE-627 \|e rakwb
041			\|a eng
050		0	\|a RG1-991
100	0		\|a Saji Philip \|e verfasserin \|4 aut
245	1	0	\|a Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
264		1	\|c 2016
336			\|a Text \|b txt \|2 rdacontent
337			\|a Computermedien \|b c \|2 rdamedia
338			\|a Online-Ressource \|b cr \|2 rdacarrier
520			\|a Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.
650		4	\|a dilated right ventricle
650		4	\|a fetal autopsy
650		4	\|a right ventricular dysplasia
650		4	\|a uhl anomaly
653		0	\|a Gynecology and obstetrics
700	0		\|a Sarasa Bharati \|e verfasserin \|4 aut
700	0		\|a Kottureth Mammen Cherian \|e verfasserin \|4 aut
700	0		\|a Saroja Bharati \|e verfasserin \|4 aut
773	0	8	\|i In \|t American Journal of Perinatology Reports \|d Thieme Medical Publishers, Inc., 2014 \|g 06(2016), 01, Seite e91-e95 \|w (DE-627)668712171 \|w (DE-600)2628594-0 \|x 21577005 \|7 nnns
773	1	8	\|g volume:06 \|g year:2016 \|g number:01 \|g pages:e91-e95
856	4	0	\|u https://doi.org/10.1055/s-0035-1566296 \|z kostenfrei
856	4	0	\|u https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 \|z kostenfrei
856	4	0	\|u http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 \|z kostenfrei
856	4	2	\|u https://doaj.org/toc/2157-6998 \|y Journal toc \|z kostenfrei
856	4	2	\|u https://doaj.org/toc/2157-7005 \|y Journal toc \|z kostenfrei
912			\|a GBV_USEFLAG_A
912			\|a SYSFLAG_A
912			\|a GBV_DOAJ
912			\|a GBV_ILN_20
912			\|a GBV_ILN_22
912			\|a GBV_ILN_23
912			\|a GBV_ILN_24
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_65
912			\|a GBV_ILN_69
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_95
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_151
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_230
912			\|a GBV_ILN_267
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_602
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_4012
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4367
912			\|a GBV_ILN_4700
951			\|a AR
952			\|d 06 \|j 2016 \|e 01 \|h e91-e95

Indexfelder

author_variant	s p sp s b sb k m c kmc s b sb
matchkey_str	article:21577005:2016----::rntligoioulnmlwtat
hierarchy_sort_str	2016
callnumber-subject-code	RG
publishDate	2016
allfields	10.1055/s-0035-1566296 doi (DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02 DE-627 ger DE-627 rakwb eng RG1-991 Saji Philip verfasserin aut Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly. dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics Sarasa Bharati verfasserin aut Kottureth Mammen Cherian verfasserin aut Saroja Bharati verfasserin aut In American Journal of Perinatology Reports Thieme Medical Publishers, Inc., 2014 06(2016), 01, Seite e91-e95 (DE-627)668712171 (DE-600)2628594-0 21577005 nnns volume:06 year:2016 number:01 pages:e91-e95 https://doi.org/10.1055/s-0035-1566296 kostenfrei https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 kostenfrei https://doaj.org/toc/2157-6998 Journal toc kostenfrei https://doaj.org/toc/2157-7005 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 06 2016 01 e91-e95
spelling	10.1055/s-0035-1566296 doi (DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02 DE-627 ger DE-627 rakwb eng RG1-991 Saji Philip verfasserin aut Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly. dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics Sarasa Bharati verfasserin aut Kottureth Mammen Cherian verfasserin aut Saroja Bharati verfasserin aut In American Journal of Perinatology Reports Thieme Medical Publishers, Inc., 2014 06(2016), 01, Seite e91-e95 (DE-627)668712171 (DE-600)2628594-0 21577005 nnns volume:06 year:2016 number:01 pages:e91-e95 https://doi.org/10.1055/s-0035-1566296 kostenfrei https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 kostenfrei https://doaj.org/toc/2157-6998 Journal toc kostenfrei https://doaj.org/toc/2157-7005 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 06 2016 01 e91-e95
allfields_unstemmed	10.1055/s-0035-1566296 doi (DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02 DE-627 ger DE-627 rakwb eng RG1-991 Saji Philip verfasserin aut Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly. dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics Sarasa Bharati verfasserin aut Kottureth Mammen Cherian verfasserin aut Saroja Bharati verfasserin aut In American Journal of Perinatology Reports Thieme Medical Publishers, Inc., 2014 06(2016), 01, Seite e91-e95 (DE-627)668712171 (DE-600)2628594-0 21577005 nnns volume:06 year:2016 number:01 pages:e91-e95 https://doi.org/10.1055/s-0035-1566296 kostenfrei https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 kostenfrei https://doaj.org/toc/2157-6998 Journal toc kostenfrei https://doaj.org/toc/2157-7005 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 06 2016 01 e91-e95
allfieldsGer	10.1055/s-0035-1566296 doi (DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02 DE-627 ger DE-627 rakwb eng RG1-991 Saji Philip verfasserin aut Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly. dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics Sarasa Bharati verfasserin aut Kottureth Mammen Cherian verfasserin aut Saroja Bharati verfasserin aut In American Journal of Perinatology Reports Thieme Medical Publishers, Inc., 2014 06(2016), 01, Seite e91-e95 (DE-627)668712171 (DE-600)2628594-0 21577005 nnns volume:06 year:2016 number:01 pages:e91-e95 https://doi.org/10.1055/s-0035-1566296 kostenfrei https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 kostenfrei https://doaj.org/toc/2157-6998 Journal toc kostenfrei https://doaj.org/toc/2157-7005 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 06 2016 01 e91-e95
allfieldsSound	10.1055/s-0035-1566296 doi (DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02 DE-627 ger DE-627 rakwb eng RG1-991 Saji Philip verfasserin aut Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly. dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics Sarasa Bharati verfasserin aut Kottureth Mammen Cherian verfasserin aut Saroja Bharati verfasserin aut In American Journal of Perinatology Reports Thieme Medical Publishers, Inc., 2014 06(2016), 01, Seite e91-e95 (DE-627)668712171 (DE-600)2628594-0 21577005 nnns volume:06 year:2016 number:01 pages:e91-e95 https://doi.org/10.1055/s-0035-1566296 kostenfrei https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 kostenfrei http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 kostenfrei https://doaj.org/toc/2157-6998 Journal toc kostenfrei https://doaj.org/toc/2157-7005 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 06 2016 01 e91-e95
language	English
source	In American Journal of Perinatology Reports 06(2016), 01, Seite e91-e95 volume:06 year:2016 number:01 pages:e91-e95
sourceStr	In American Journal of Perinatology Reports 06(2016), 01, Seite e91-e95 volume:06 year:2016 number:01 pages:e91-e95
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly Gynecology and obstetrics
isfreeaccess_bool	true
container_title	American Journal of Perinatology Reports
authorswithroles_txt_mv	Saji Philip @@aut@@ Sarasa Bharati @@aut@@ Kottureth Mammen Cherian @@aut@@ Saroja Bharati @@aut@@
publishDateDaySort_date	2016-01-01T00:00:00Z
hierarchy_top_id	668712171
id	DOAJ074821601
language_de	englisch
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ074821601</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230309130600.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230228s2016 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1055/s-0035-1566296</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ074821601</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RG1-991</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Saji Philip</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2016</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">dilated right ventricle</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">fetal autopsy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">right ventricular dysplasia</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">uhl anomaly</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Gynecology and obstetrics</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Sarasa Bharati</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Kottureth Mammen Cherian</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Saroja Bharati</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">American Journal of Perinatology Reports</subfield><subfield code="d">Thieme Medical Publishers, Inc., 2014</subfield><subfield code="g">06(2016), 01, Seite e91-e95</subfield><subfield code="w">(DE-627)668712171</subfield><subfield code="w">(DE-600)2628594-0</subfield><subfield code="x">21577005</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:06</subfield><subfield code="g">year:2016</subfield><subfield code="g">number:01</subfield><subfield code="g">pages:e91-e95</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1055/s-0035-1566296</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2157-6998</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2157-7005</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_267</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">06</subfield><subfield code="j">2016</subfield><subfield code="e">01</subfield><subfield code="h">e91-e95</subfield></datafield></record></collection>
callnumber-first	R - Medicine
author	Saji Philip
spellingShingle	Saji Philip misc RG1-991 misc dilated right ventricle misc fetal autopsy misc right ventricular dysplasia misc uhl anomaly misc Gynecology and obstetrics Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
authorStr	Saji Philip
ppnlink_with_tag_str_mv	@@773@@(DE-627)668712171
format	electronic Article
delete_txt_mv	keep
author_role	aut aut aut aut
collection	DOAJ
remote_str	true
callnumber-label	RG1-991
illustrated	Not Illustrated
issn	21577005
topic_title	RG1-991 Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation dilated right ventricle fetal autopsy right ventricular dysplasia uhl anomaly
topic	misc RG1-991 misc dilated right ventricle misc fetal autopsy misc right ventricular dysplasia misc uhl anomaly misc Gynecology and obstetrics
topic_unstemmed	misc RG1-991 misc dilated right ventricle misc fetal autopsy misc right ventricular dysplasia misc uhl anomaly misc Gynecology and obstetrics
topic_browse	misc RG1-991 misc dilated right ventricle misc fetal autopsy misc right ventricular dysplasia misc uhl anomaly misc Gynecology and obstetrics
format_facet	Elektronische Aufsätze Aufsätze Elektronische Ressource
format_main_str_mv	Text Zeitschrift/Artikel
carriertype_str_mv	cr
hierarchy_parent_title	American Journal of Perinatology Reports
hierarchy_parent_id	668712171
hierarchy_top_title	American Journal of Perinatology Reports
isfreeaccess_txt	true
familylinks_str_mv	(DE-627)668712171 (DE-600)2628594-0
title	Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
ctrlnum	(DE-627)DOAJ074821601 (DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02
title_full	Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
author_sort	Saji Philip
journal	American Journal of Perinatology Reports
journalStr	American Journal of Perinatology Reports
callnumber-first-code	R
lang_code	eng
isOA_bool	true
recordtype	marc
publishDateSort	2016
contenttype_str_mv	txt
author_browse	Saji Philip Sarasa Bharati Kottureth Mammen Cherian Saroja Bharati
container_volume	06
class	RG1-991
format_se	Elektronische Aufsätze
author-letter	Saji Philip
doi_str_mv	10.1055/s-0035-1566296
author2-role	verfasserin
title_sort	prenatal diagnosis of uhl anomaly with autopsy correlation
callnumber	RG1-991
title_auth	Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
abstract	Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.
abstractGer	Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.
abstract_unstemmed	Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.
collection_details	GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_267 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700
container_issue	01
title_short	Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation
url	https://doi.org/10.1055/s-0035-1566296 https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02 http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296 https://doaj.org/toc/2157-6998 https://doaj.org/toc/2157-7005
remote_bool	true
author2	Sarasa Bharati Kottureth Mammen Cherian Saroja Bharati
author2Str	Sarasa Bharati Kottureth Mammen Cherian Saroja Bharati
ppnlink	668712171
callnumber-subject	RG - Gynecology and Obstetrics
mediatype_str_mv	c
isOA_txt	true
hochschulschrift_bool	false
doi_str	10.1055/s-0035-1566296
callnumber-a	RG1-991
up_date	2024-07-04T00:43:42.151Z
_version_	1803607156616855552
fullrecord_marcxml	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ074821601</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230309130600.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230228s2016 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1055/s-0035-1566296</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ074821601</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ318505d89a0a4ef78f5739803df7ae02</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RG1-991</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Saji Philip</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2016</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Uhl anomaly is a rare form of congenital hypoplasia of the right ventricular myocardium. Here, we report, a rare finding in fetal cardiac ultrasound in a 33-year-old woman who presented at 20 weeks' of gestation. A diagnosis of Uhl anomaly was made. An autopsy was performed at 23weeks gestation after obtaining permission for medicolegal termination of pregnancy. Histopathological examination confirmed the diagnosis. Diagnosing Uhl anomaly in fetal life is essential since mortality and survival mainly depend on the severity of right ventricle dysfunction related to, the either partial or complete absence of the myocardium. Hence, surviving cases need to be followed up carefully and counselled accordingly.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">dilated right ventricle</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">fetal autopsy</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">right ventricular dysplasia</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">uhl anomaly</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Gynecology and obstetrics</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Sarasa Bharati</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Kottureth Mammen Cherian</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="0" ind2=" "><subfield code="a">Saroja Bharati</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">American Journal of Perinatology Reports</subfield><subfield code="d">Thieme Medical Publishers, Inc., 2014</subfield><subfield code="g">06(2016), 01, Seite e91-e95</subfield><subfield code="w">(DE-627)668712171</subfield><subfield code="w">(DE-600)2628594-0</subfield><subfield code="x">21577005</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:06</subfield><subfield code="g">year:2016</subfield><subfield code="g">number:01</subfield><subfield code="g">pages:e91-e95</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1055/s-0035-1566296</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doaj.org/article/318505d89a0a4ef78f5739803df7ae02</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://www.thieme-connect.de/DOI/DOI?10.1055/s-0035-1566296</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2157-6998</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="u">https://doaj.org/toc/2157-7005</subfield><subfield code="y">Journal toc</subfield><subfield code="z">kostenfrei</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_DOAJ</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_20</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_22</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_23</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_24</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_39</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_40</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_62</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_63</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_65</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_69</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_95</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_105</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_110</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_151</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_161</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_170</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_206</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_213</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_230</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_267</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_285</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_293</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_602</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2014</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4037</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4112</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4125</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4126</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4249</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4305</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4306</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4307</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4313</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4322</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4323</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4324</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4325</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4338</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4367</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4700</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">06</subfield><subfield code="j">2016</subfield><subfield code="e">01</subfield><subfield code="h">e91-e95</subfield></datafield></record></collection>
score	7.399535

Nicht das Richtige dabei?

Schreiben Sie uns!

Prenatal Diagnosis of Uhl Anomaly with Autopsy Correlation

Nicht das Richtige dabei?

Zugang & Verfügbarkeit

Vorhandene Bände

Nicht das Richtige dabei?