Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39-Reference-Cited by-同舟云学术

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Published:2009-07 Issue:1 Volume:85 Page:25-39
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Schultz Julie M.,Khan Shaheen N.,Ahmed Zubair M.,Riazuddin Saima,Waryah Ali M.,Chhatre Dhananjay,Starost Matthew F.,Ploplis Barbara,Buckley Stephanie,Velásquez David,Kabra Madhulika,Lee Kwanghyuk,Hassan Muhammad J.,Ali Ghazanfar,Ansar Muhammad,Ghosh Manju,Wilcox Edward R.,Ahmad Wasim,Merlino Glenn,Leal Suzanne M.,Riazuddin Sheikh,Friedman Thomas B.,Morell Robert J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference81 articles.

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2. Recent advances in the understanding of syndromic forms of hearing loss;Friedman;Ear Hear.,2003

3. Sex-linked deafness;Petersen;Clin. Genet.,2008

4. Non-syndromic, autosomal-recessive deafness;Petersen;Clin. Genet.,2006

5. Molecular genetics of hearing loss;Petit;Annu. Rev. Genet.,2001

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