Single gene influences on radiologically-detectable malformations of the inner ear

Journal of Communication Disorders

Volumn 31, Issue 5, 1998, Pages 391-410

  Smith, Shelley D ^a,b   Harker, Lee A ^a  

^a CREIGHTON UNIVERSITY   (United States)

^b BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRANCHIOOTORENAL SYNDROME; COCHLEA; DIGEORGE SYNDROME; DISEASE CLASSIFICATION; GENETICS; HEARING LOSS; HUMAN; INNER EAR MALFORMATION; MANDIBULOFACIAL DYSOSTOSIS; PATHOGENESIS; PENDRED SYNDROME; REVIEW; VESTIBULAR DISORDER; VESTIBULE AQUEDUCT; WAARDENBURG SYNDROME;

EID: 0032169497     PISSN: 00219924     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-9924(98)00012-4     Document Type: Article

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