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Volumn 46, Issue 5, 2005, Pages 797-800

Molecular analysis in diagnostic procedure of hearing impairment in newborns

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CROATIA; EVOKED BRAIN STEM AUDITORY RESPONSE; EVOKED OTOACOUSTIC EMISSION; GENE DELETION; GENE MUTATION; GENETIC COUNSELING; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN SCREENING; POLYMERASE CHAIN REACTION;

EID: 26244431686     PISSN: 03539504     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (21)
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    • Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss
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  • 11
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  • 13
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.