Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome-Reference-Cited by-同舟云学术

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Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome

Published:2004-05-27 Issue:23 Volume:101 Page:8652-8657
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Twigg S. R. F.,Kan R.,Babbs C.,Bochukova E. G.,Robertson S. P.,Wall S. A.,Morriss-Kay G. M.,Wilkie A. O. M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference32 articles.

1. Craniofrontonasal dysplasia: clinical and genetic analysis

2. Delineation of the male phenotype in craniofrontonasal syndrome

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