Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families

BACKGROUND: Syndactyly type 1 (SD1) is an autosomal dominant limb malformation characterized in its classical form by complete or partial webbing between the third and fourth fingers and/or the second and third toes. Its four subtypes (a, b, c, and d) are defined based on variable phenotypes, but th...

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Bibliographic Details
Main Authors:	Dai, Limeng, Liu, Dan, Song, Min, Xu, Xueqing, Xiong, Gang, Yang, Kang, Zhang, Kun, Meng, Hui, Guo, Hong, Bai, Yun
Format:	Artigo
Language:	Inglês
Published:	Public Library of Science 2014
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4006867/ https://ncbi.nlm.nih.gov/pubmed/24789103 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0096192
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Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families

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