Microarray-based mutation detection of pediatric sporadic nonsyndromic hearing loss in China

International Journal of Pediatric Otorhinolaryngology

Volumn 76, Issue 2, 2012, Pages 235-239

  Qu, Chunyan ^a   Sun, Xibin ^a   Shi, Yang ^a   Gong, Angela ^b   Liang, Shuang ^a   Zhao, Min ^a   Chen, Yan ^a   Liang, Fenghe ^c  

^a China Disabled Persons' Federation Information Center   (China)

^b Gouverneur Healthcare Hospital   (United States)

^c CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

12s rRNA; GJB2; Hearing loss; Pendred syndrome; SLC26A4

Indexed keywords

RNA 12S;

ADOLESCENT; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; GENE; GENE DELETION; GENE MUTATION; GENETIC SCREENING; GJB2 GENE; GJB3 GENE; HEARING LOSS; HEREDITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MICROARRAY ANALYSIS; MUTATIONAL ANALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SLC26A4 GENE; SPORADIC NONSYNDROMIC HEARING LOSS;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; COHORT STUDIES; CONNEXINS; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS, SENSORINEURAL; HUMANS; INCIDENCE; INFANT; MALE; MICROARRAY ANALYSIS; MUTATION; RECEPTORS, SOMATOSTATIN; RISK ASSESSMENT; SEVERITY OF ILLNESS INDEX;

EID: 84855926523     PISSN: 01655876     EISSN: 18728464     Source Type: Journal    
DOI: 10.1016/j.ijporl.2011.11.009     Document Type: Article

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