An overview of hereditary hearing loss

ORL

Volumn 68, Issue 2, 2006, Pages 57-63

  Bayazit, Yildirim A ^a   Yilmaz, Metin ^a  

^a GAZI UNIVERSITY   (Turkey)

Author keywords

Hereditary hearing loss; Mitochondrial hearing loss; Nonsyndromic hearing loss; Syndromic hearing loss; X linked hearing loss

Indexed keywords

ALLELE; ALPORT SYNDROME; BIOTINIDASE DEFICIENCY; BRANCHIOOTORENAL SYNDROME; GENE LOCUS; GENETIC DISORDER; GENETIC POLYMORPHISM; GENOME; GENOTYPE; HEARING LOSS; HEREDITY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LONG QT SYNDROME; MITOCHONDRION; NONHUMAN; NORRIE DISEASE; PENDRED SYNDROME; PHENOTYPE; PRIORITY JOURNAL; REVIEW; USHER SYNDROME; WAARDENBURG SYNDROME; X CHROMOSOME LINKAGE;

ALLELES; DNA, MITOCHONDRIAL; GENETIC HETEROGENEITY; GENOTYPE; HEARING LOSS; HUMANS; INHERITANCE PATTERNS; PHENOTYPE; POLYMORPHISM, GENETIC; SYNDROME;

EID: 33644883054     PISSN: 03011569     EISSN: None     Source Type: Journal    
DOI: 10.1159/000091090     Document Type: Review

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