Exome sequencing and genome-wide copy number variant...

BMC Genomics 2014 / 12 Vol. 15; Iss. 1

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

Haraksingh, Rajini R, Jahanbani, Fereshteh, Rodriguez-Paris, Juan, Gelernter, Joel, Nadeau, Kari C, Oghalai, John S, Schrijver, Iris, Snyder, Michael P
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Volume:
15
Language:
english
Journal:
BMC Genomics
DOI:
10.1186/1471-2164-15-1155
Date:
December, 2014
File:
PDF, 1.29 MB
english, 2014
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