Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome

Author:

Kalatzis Vasiliki,Abdelhak Sonia,Compain Sylvie,Vincent Christophe,Petit Christine

Publisher

Elsevier BV

Subject

Genetics

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Syndromic Hearing Loss: A Brief Review of Common Presentations and Genetics;Journal of Pediatric Genetics;2018-01-04

2. Branchiootorenal syndrome: A case report;Nigerian Postgraduate Medical Journal;2018

3. The Branchio-oto-renal Syndrome;Genetic Diseases of the Kidney;2009

4. Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome;The American Journal of Human Genetics;2007-04

5. Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome;European Journal of Human Genetics;2002-10-29

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