Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia-Reference-Cited by-同舟云学术

Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

Published:2007-02 Issue:2 Volume:80 Page:338-344
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Tekin Mustafa,Hişmi Burcu Öztürk,Fitoz Suat,Özdağ Hilal,Cengiz Filiz Başak,Sırmacı Aslı,Aslan İdil,İnceoğlu Bora,Yüksel-Konuk E. Berrin,Yılmaz Seda Taşır,Yasun Öztan,Akar Nejat

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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5. Genetic hearing loss associated with external ear abnormalities;Allanson,2004

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