Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin
[Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous famili...
Ausführliche Beschreibung
Gespeichert in:
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
s.l.: Nature Publishing Group ; 2001 |
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| Umfang: |
3 |
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| Reproduktion: |
Nature Archives 1869 - 2009 |
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| Übergeordnetes Werk: |
In: Nature genetics - New York, NY : Nature America, 1992, 29(2001), 2 vom: Jan., Seite 134-136 |
| Übergeordnetes Werk: |
volume:29 ; year:2001 ; number:2 ; month:01 ; pages:134-136 ; extent:3 |
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|---|
| DOI / URN: |
10.1038/ng716 |
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10.1038/ng716 doi (DE-627)NLEJ231748264 DE-627 ger DE-627 rakwb eng XD-US Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin [s.l.] Nature Publishing Group 2001 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... Nature Archives 1869 - 2009 Bergman, Reuven oth Richard, Gabriele oth Lurie, Raziel oth Shalev, Stavit oth Petronius, Dan oth Shalata, Adel oth Anbinder, Yefim oth Leibu, Rina oth Perlman, Ido oth Cohen, Nadine oth Szargel, Raymonde oth Sprecher, Eli oth In Nature genetics New York, NY : Nature America, 1992 29(2001), 2 vom: Jan., Seite 134-136 (DE-627)NLEJ227682351 (DE-600)1494946-5 1546-1718 nnns volume:29 year:2001 number:2 month:01 pages:134-136 extent:3 http://dx.doi.org/10.1038/ng716 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 29 2001 2 1 134-136 3 |
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10.1038/ng716 doi (DE-627)NLEJ231748264 DE-627 ger DE-627 rakwb eng XD-US Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin [s.l.] Nature Publishing Group 2001 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... Nature Archives 1869 - 2009 Bergman, Reuven oth Richard, Gabriele oth Lurie, Raziel oth Shalev, Stavit oth Petronius, Dan oth Shalata, Adel oth Anbinder, Yefim oth Leibu, Rina oth Perlman, Ido oth Cohen, Nadine oth Szargel, Raymonde oth Sprecher, Eli oth In Nature genetics New York, NY : Nature America, 1992 29(2001), 2 vom: Jan., Seite 134-136 (DE-627)NLEJ227682351 (DE-600)1494946-5 1546-1718 nnns volume:29 year:2001 number:2 month:01 pages:134-136 extent:3 http://dx.doi.org/10.1038/ng716 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 29 2001 2 1 134-136 3 |
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10.1038/ng716 doi (DE-627)NLEJ231748264 DE-627 ger DE-627 rakwb eng XD-US Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin [s.l.] Nature Publishing Group 2001 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... Nature Archives 1869 - 2009 Bergman, Reuven oth Richard, Gabriele oth Lurie, Raziel oth Shalev, Stavit oth Petronius, Dan oth Shalata, Adel oth Anbinder, Yefim oth Leibu, Rina oth Perlman, Ido oth Cohen, Nadine oth Szargel, Raymonde oth Sprecher, Eli oth In Nature genetics New York, NY : Nature America, 1992 29(2001), 2 vom: Jan., Seite 134-136 (DE-627)NLEJ227682351 (DE-600)1494946-5 1546-1718 nnns volume:29 year:2001 number:2 month:01 pages:134-136 extent:3 http://dx.doi.org/10.1038/ng716 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 29 2001 2 1 134-136 3 |
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10.1038/ng716 doi (DE-627)NLEJ231748264 DE-627 ger DE-627 rakwb eng XD-US Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin [s.l.] Nature Publishing Group 2001 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... Nature Archives 1869 - 2009 Bergman, Reuven oth Richard, Gabriele oth Lurie, Raziel oth Shalev, Stavit oth Petronius, Dan oth Shalata, Adel oth Anbinder, Yefim oth Leibu, Rina oth Perlman, Ido oth Cohen, Nadine oth Szargel, Raymonde oth Sprecher, Eli oth In Nature genetics New York, NY : Nature America, 1992 29(2001), 2 vom: Jan., Seite 134-136 (DE-627)NLEJ227682351 (DE-600)1494946-5 1546-1718 nnns volume:29 year:2001 number:2 month:01 pages:134-136 extent:3 http://dx.doi.org/10.1038/ng716 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 29 2001 2 1 134-136 3 |
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10.1038/ng716 doi (DE-627)NLEJ231748264 DE-627 ger DE-627 rakwb eng XD-US Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin [s.l.] Nature Publishing Group 2001 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... Nature Archives 1869 - 2009 Bergman, Reuven oth Richard, Gabriele oth Lurie, Raziel oth Shalev, Stavit oth Petronius, Dan oth Shalata, Adel oth Anbinder, Yefim oth Leibu, Rina oth Perlman, Ido oth Cohen, Nadine oth Szargel, Raymonde oth Sprecher, Eli oth In Nature genetics New York, NY : Nature America, 1992 29(2001), 2 vom: Jan., Seite 134-136 (DE-627)NLEJ227682351 (DE-600)1494946-5 1546-1718 nnns volume:29 year:2001 number:2 month:01 pages:134-136 extent:3 http://dx.doi.org/10.1038/ng716 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 29 2001 2 1 134-136 3 |
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[Auszug] Congenital hypotrichosis associated with juvenile macular dystrophy (HJMD; MIM601553) is an autosomal recessive disorder of unknown etiology, characterized by hair loss heralding progressive macular degeneration and early blindness. We used homozygosity mapping in four consanguineous families to ... |
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