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;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

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Brownstein, Zippora
Friedman, Lilach M.
Shahin, Hashem
Oron-Karni, Varda
Kol, Nitzan
Abu Rayyan, Amal
Parzefall, Thomas
Lev, Dorit
Shalev, Stavit
Frydman, Moshe
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Shohat, Mordechai
Rahile, Michele
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