Twenty-six novelEFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)-Reference-Cited by-同舟云学术

Twenty-six novelEFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)

Published:2005 Issue:2 Volume:26 Page:113-118
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Wieland Ilse,Reardon William,Jakubiczka Sibylle,Franco Brunella,Kress Wolfram,Vincent-Delorme Catherine,Thierry Patrick,Edwards Matt,König Rainer,Rusu Cristina,Schweiger Susann,Thompson Elizabeth,Tinschert Sigrid,Stewart Fiona,Wieacker Peter

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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4. Ephrin-B1 forward and reverse signaling are required during mouse development

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