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

被引：0
|
作者：
Zippora Brownstein
Lilach M Friedman
Hashem Shahin
Varda Oron-Karni
Nitzan Kol
Amal Abu Rayyan
Thomas Parzefall
Dorit Lev
Stavit Shalev
Moshe Frydman
Bella Davidov
Mordechai Shohat
Michele Rahile
Sari Lieberman
Ephrat Levy-Lahad
Ming K Lee
Noam Shomron
Mary-Claire King
Tom Walsh
Moien Kanaan
Karen B Avraham
机构：
[1] Sackler Faculty of Medicine,Department of Human Molecular Genetics and Biochemistry
[2] Tel Aviv University,Department of Biological Sciences
[3] Bethlehem University,Department of Medical Genetics
[4] Bethlehem,Department of Medicine (Medical Genetics) and Department of Genome Sciences
[5] Genome High-Throughput Sequencing Laboratory,Department of Cell and Developmental Biology
[6] Tel Aviv University,undefined
[7] Institute of Medical Genetics,undefined
[8] Wolfson Medical Center,undefined
[9] Genetics Institute,undefined
[10] Ha'Emek Medical Center,undefined
[11] Rappaport Faculty of Medicine,undefined
[12] Technion-Israel Institute of Technology,undefined
[13] Danek Gartner Institute of Human Genetics,undefined
[14] Sheba Medical Center,undefined
[15] Rabin Medical Center,undefined
[16] Darr Al Kalima Audiological Clinic,undefined
[17] Medical Genetics Institute,undefined
[18] Shaare Zedek Medical Center,undefined
[19] Hebrew University Medical School,undefined
[20] University of Washington,undefined
[21] Sackler Faculty of Medicine,undefined
[22] Tel Aviv University,undefined
来源：
Genome Biology | / 12卷
关键词：
Hearing Loss; Massively Parallel Sequencing; Deaf Individual; Wolfram Syndrome; Deafness Gene;
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