학술논문
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
Document Type
Article
Author
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, 2009, 17(1):14-21)
Subject
Language
English
ISSN
10184813
14765438
14765438