Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing

Proceedings of the National Academy of Sciences of the United States of America

Volumn 107, Issue 49, 2010, Pages 21104-21109

  Shearer, A Eliot ^a   DeLuca, Adam P ^b,c   Hildebrand, Michael S ^a   Taylor, Kyle R ^b,c   Gurrola II, José ^a   Scherer, Steve ^d   Scheetz, Todd E ^a,b,c   Smith, Richard J H ^a,c  

^a UNIVERSITY OF IOWA   (United States)

^b IA United States   (United States)

^c UNIVERSITY OF IOWA   (United States)

^d BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Deafness; Diagnostics; Genomics; Next generation sequencing; Usher syndrome

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONGENITAL DEAFNESS; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DEVICE; DIAGNOSTIC TEST; DIAGNOSTIC TEST ACCURACY STUDY; GENE SEQUENCE; GENE TECHNOLOGY; GENETIC SCREENING; HUMAN; PRIORITY JOURNAL; REPRODUCIBILITY; SENSITIVITY AND SPECIFICITY; SINGLE NUCLEOTIDE POLYMORPHISM;

DNA MUTATIONAL ANALYSIS; GENETIC TESTING; GENOTYPE; HEARING LOSS; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 78650506429     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1012989107     Document Type: Article

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