Author:
Tekin M,Öztürkmen Akay H,Fitoz S,Birnbaum S,Cengiz FB,Sennaroğlu L,İncesulu A,Yüksel Konuk EB,Hasanefendioğlu Bayrak A,Şentürk S,Cebeci İ,Ütine GE,Tunçbilek E,Nance WE,Duman D
Subject
Genetics(clinical),Genetics
Reference30 articles.
1. Michel’s anomaly, type I microtia and microdontia;Hersh;Ear Nose Throat J,1991
2. Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia;Tekin;Am J Hum Genet,2007
3. Memoire sur les anomalies congenitales de poreille intern;Michel;Gazette Med de Strasburg,1863
4. CT and MR findings of Michel anomaly: inner ear aplasia;Marsot-Dupuch;AJNR Am J Neuroradiol,1999
5. Three familial cases of Michel’s aplasia;Daneshi;Otol Neurotol,2002
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