Next-Generation Sequencing in Genetic Hearing Loss-Reference-Cited by-同舟云学术

Next-Generation Sequencing in Genetic Hearing Loss

Published:2013-08 Issue:8 Volume:17 Page:581-587
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Yan Denise¹,Tekin Mustafa²,Blanton Susan H.²,Liu Xue Zhong¹²

Affiliation:

1. Department of Otolaryngology, Miller School of Medicine, University of Miami, Miami, Florida.

2. Dr. John T. Macdonald Department of Human Genetics, John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2012.0464

Reference46 articles.

1. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

2. Linkage of a gene for dominant non-syndromic deafness to chromosome 19

3. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

4. Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

5. Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

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