Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia
- 1 February 2007
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 80 (2) , 338-344
- https://doi.org/10.1086/510920
Abstract
No abstract availableKeywords
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