DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance?

Advances in oto-rhino-laryngology

Volumn 56, Issue , 2000, Pages 171-175

  Chen, A H ^a   Fukushima, K ^a   McGuirt, W T ^a   Smith, R J ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19; CHROMOSOME 3; CHROMOSOME MAP; GENETIC LINKAGE; GENETICS; HEARING IMPAIRMENT; HUMAN; PATHOPHYSIOLOGY; PERCEPTION DEAFNESS; RECESSIVE GENE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 3; DEAFNESS; GENES, RECESSIVE; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS);

MLCS; MLOWN;

EID: 0033655236     PISSN: 00653071     EISSN: None     Source Type: Journal    
DOI: 10.1159/000059089     Document Type: Article

References (0)