Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families-Reference-Cited by-同舟云学术

Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families

Published:2011 Issue:9 Volume:12 Page:R89
ISSN:1465-6906
Container-title:Genome Biology
language:en
Short-container-title:Genome Biol

Author:

Brownstein Zippora,Friedman Lilach M,Shahin Hashem,Oron-Karni Varda,Kol Nitzan,Rayyan Amal,Parzefall Thomas,Lev Dorit,Shalev Stavit,Frydman Moshe,Davidov Bella,Shohat Mordechai,Rahile Michele,Lieberman Sari,Levy-Lahad Ephrat,Lee Ming K,Shomron Noam,King Mary-Claire,Walsh Tom,Kanaan Moien,Avraham Karen B

Publisher

Springer Science and Business Media LLC

Reference33 articles.

1. The genetics of deafness

2. Deafness Genes in Israel: Implications for Diagnostics in the Clinic

3. Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

4. Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

5. Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84

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