Newborn hearing screening and genetic testing in 8974 Brazilian neonates

International Journal of Pediatric Otorhinolaryngology

Volumn 74, Issue 8, 2010, Pages 926-929

  Nivoloni, Karin de A B ^a   da Silva Costa, Sueli M ^b   Pomílio, Mariza C A ^a   Pereira, Tânia ^a   Lopes, Karen de C ^a   de Moraes, Vanessa C S ^b   Alexandrino, Fabiana ^b   de Oliveira, Camila A ^b   Sartorato, Edi L ^b  

^a Associação Terapêutica de Estimulação Auditiva e Linguagem ATEAL   (Brazil)

^b UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

35delG mutation; Aminoglycosides; Deafness; Hearing loss; Mitochondrial mutation; Newborns

Indexed keywords

ADENINE; CONNEXIN 26; GUANINE; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN; PROTEIN MTRNR1; UNCLASSIFIED DRUG;

ARTICLE; AUDITORY SCREENING; BRAZIL; EARLY DIAGNOSIS; GENE DELETION; GENE MUTATION; GENETIC SCREENING; HEARING IMPAIRMENT; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MITOCHONDRIAL GENE; NEWBORN; NEWBORN SCREENING; OTOACOUSTIC EMISSION; PRIORITY JOURNAL;

BRAZIL; CONNEXINS; DEAFNESS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HEARING LOSS; HEARING TESTS; HUMANS; INCIDENCE; INFANT, NEWBORN; MALE; MUTATION; NEONATAL SCREENING; OTOACOUSTIC EMISSIONS, SPONTANEOUS; RISK ASSESSMENT;

EID: 77953913052     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijporl.2010.05.015     Document Type: Article

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