Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome
[Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ......
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Englisch |
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s.l.: Macmillian Magazines Ltd. ; 2003 |
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6 |
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Nature Archives 1869 - 2009 |
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| Übergeordnetes Werk: |
In: Nature |
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volume:425 ; year:2003 ; number:6958 ; month:00 ; pages:628-633 ; extent:6 |
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10.1038/nature02030 |
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| 520 | |a [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... | ||
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10.1038/nature02030 doi (DE-627)NLEJ234792248 DE-627 ger DE-627 rakwb eng Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome [s.l.] Macmillian Magazines Ltd. 2003 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... Nature Archives 1869 - 2009 Ansley, Stephen J. oth Badano, Jose L. oth Blacque, Oliver E. oth Hill, Josephine oth Hoskins, Bethan E. oth Leitch, Carmen C. oth Chul Kim, Jun oth Ross, Alison J. oth Eichers, Erica R. oth Teslovich, Tanya M. oth Mah, Allan K. oth Johnsen, Robert C. oth Cavender, John C. oth Alan Lewis, Richard oth Leroux, Michel R. oth Beales, Philip L. oth Katsanis, Nicholas oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 425(2003), 6958, Seite 628-633 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:425 year:2003 number:6958 month:00 pages:628-633 extent:6 http://dx.doi.org/10.1038/nature02030 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 425 2003 6958 0 628-633 6 |
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10.1038/nature02030 doi (DE-627)NLEJ234792248 DE-627 ger DE-627 rakwb eng Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome [s.l.] Macmillian Magazines Ltd. 2003 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... Nature Archives 1869 - 2009 Ansley, Stephen J. oth Badano, Jose L. oth Blacque, Oliver E. oth Hill, Josephine oth Hoskins, Bethan E. oth Leitch, Carmen C. oth Chul Kim, Jun oth Ross, Alison J. oth Eichers, Erica R. oth Teslovich, Tanya M. oth Mah, Allan K. oth Johnsen, Robert C. oth Cavender, John C. oth Alan Lewis, Richard oth Leroux, Michel R. oth Beales, Philip L. oth Katsanis, Nicholas oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 425(2003), 6958, Seite 628-633 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:425 year:2003 number:6958 month:00 pages:628-633 extent:6 http://dx.doi.org/10.1038/nature02030 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 425 2003 6958 0 628-633 6 |
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10.1038/nature02030 doi (DE-627)NLEJ234792248 DE-627 ger DE-627 rakwb eng Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome [s.l.] Macmillian Magazines Ltd. 2003 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... Nature Archives 1869 - 2009 Ansley, Stephen J. oth Badano, Jose L. oth Blacque, Oliver E. oth Hill, Josephine oth Hoskins, Bethan E. oth Leitch, Carmen C. oth Chul Kim, Jun oth Ross, Alison J. oth Eichers, Erica R. oth Teslovich, Tanya M. oth Mah, Allan K. oth Johnsen, Robert C. oth Cavender, John C. oth Alan Lewis, Richard oth Leroux, Michel R. oth Beales, Philip L. oth Katsanis, Nicholas oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 425(2003), 6958, Seite 628-633 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:425 year:2003 number:6958 month:00 pages:628-633 extent:6 http://dx.doi.org/10.1038/nature02030 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 425 2003 6958 0 628-633 6 |
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10.1038/nature02030 doi (DE-627)NLEJ234792248 DE-627 ger DE-627 rakwb eng Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome [s.l.] Macmillian Magazines Ltd. 2003 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... Nature Archives 1869 - 2009 Ansley, Stephen J. oth Badano, Jose L. oth Blacque, Oliver E. oth Hill, Josephine oth Hoskins, Bethan E. oth Leitch, Carmen C. oth Chul Kim, Jun oth Ross, Alison J. oth Eichers, Erica R. oth Teslovich, Tanya M. oth Mah, Allan K. oth Johnsen, Robert C. oth Cavender, John C. oth Alan Lewis, Richard oth Leroux, Michel R. oth Beales, Philip L. oth Katsanis, Nicholas oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 425(2003), 6958, Seite 628-633 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:425 year:2003 number:6958 month:00 pages:628-633 extent:6 http://dx.doi.org/10.1038/nature02030 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 425 2003 6958 0 628-633 6 |
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10.1038/nature02030 doi (DE-627)NLEJ234792248 DE-627 ger DE-627 rakwb eng Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome [s.l.] Macmillian Magazines Ltd. 2003 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... Nature Archives 1869 - 2009 Ansley, Stephen J. oth Badano, Jose L. oth Blacque, Oliver E. oth Hill, Josephine oth Hoskins, Bethan E. oth Leitch, Carmen C. oth Chul Kim, Jun oth Ross, Alison J. oth Eichers, Erica R. oth Teslovich, Tanya M. oth Mah, Allan K. oth Johnsen, Robert C. oth Cavender, John C. oth Alan Lewis, Richard oth Leroux, Michel R. oth Beales, Philip L. oth Katsanis, Nicholas oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 425(2003), 6958, Seite 628-633 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:425 year:2003 number:6958 month:00 pages:628-633 extent:6 http://dx.doi.org/10.1038/nature02030 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 425 2003 6958 0 628-633 6 |
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[Auszug] Bardet–Biedl syndrome (BBS) is a genetically heterogeneous disorder characterized primarily by retinal dystrophy, obesity, polydactyly, renal malformations and learning disabilities. Although five BBS genes have been cloned, the molecular basis of this syndrome remains elusive. Here we ... |
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