Hypo-FunctionalSLC26A4variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?-Reference-Cited by-同舟云学术

Hypo-FunctionalSLC26A4variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?

Published:2009-04 Issue:4 Volume:30 Page:599-608
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Choi Byung Yoon,Stewart Andrew K.,Madeo Anne C.,Pryor Shannon P.,Lenhard Suzanne,Kittles Rick,Eisenman David,Jeffrey Kim H.,Niparko John,Thomsen James,Arnos Kathleen S.,Nance Walter E.,King Kelly A.,Zalewski Christopher K.,Brewer Carmen C.,Shawker Thomas,Reynolds James C.,Butman John A.,Karniski Lawrence P.,Alper Seth L.,Griffith Andrew J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference53 articles.

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3. Goitre and hearing impairment in a patient with Pendred syndrome;Arwert;Neth J Med,2008

4. Genotype-phenotype correlations for SLC26A4-related deafness;Azaiez;Hum Genet,2007

5. Dissection of epistasis in oligogenic Bardet-Biedl syndrome;Badano;Nature,2006

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