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E. Berrin Yüksel-Konuk

Ankara University

3

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Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

2009 International Journal of Pediatric Otorhinolaryngology
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A New SOX9 Gene Mutation in A Case of Campomelic Dysplasia

2009 Turkiye Klinikleri Journal of Pediatrics
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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

2007 American Journal of Human Genetics
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