Open AccessProposta de genes relacionados à deficiência auditiva sindrômica baseada em Variações do Número de Cópias (CNVs) e Perda de Heterozigose (LOH)
Author(s) -
Harumy Andrade Sakata
Publication year - 2016
Language(s) - Portuguese
Resource type - Dissertations/theses
DOI - 10.26512/2016.03.d.21104
Subject(s) - hearing loss , etiology , copy number variation , loss of heterozygosity , medical genetics , genetics , craniofacial , microarray , biology , medicine , audiology , gene , pathology , genome , allele , gene expression
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom