Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia (Q24680303)
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scientific article
Language | Label | Description | Also known as |
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English | Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia |
scientific article |
Statements
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia (English)
Burcu Oztürk Hişmi
Suat Fitoz
Filiz Başak Cengiz
Asli Sirmaci
Idil Aslan
E Berrin Yüksel-Konuk
Seda Taşir Yilmaz
Oztan Yasun
Nejat Akar
27 December 2006
1 reference