Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

标题
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
作者
关键词
-
出版物
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 17, Issue 1, Pages 14-21
出版商
Springer Nature
发表日期
2008-08-13
DOI
10.1038/ejhg.2008.141

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