A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24

American Journal of Human Genetics

Volumn 60, Issue 5, 1997, Pages 1168-1173

  Verhoeven, Kristien ^a   Van Camp, Guy ^a   Govaerts, Paul J ^b   Balemans, Wendy ^a   Schatteman, Isabelle ^a   Verstreken, Margriet ^a   Van Laer, Lut ^a   Smith, Richard J H ^c   Brown, Matthew R ^c   Van De Heyning, Paul H ^a   Somers, Thomas ^b   Offeciers, F Erwin ^b   Willems, Patrick J ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b SINT AUGUSTINUS HOSPITAL   (Belgium)

^c UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; ARTICLE; CHROMOSOME 11Q; CLINICAL ARTICLE; GENE MUTATION; GENETIC LINKAGE; HEARING LOSS; HUMAN; LANGUAGE DEVELOPMENT; PEDIGREE ANALYSIS; PRIORITY JOURNAL; TINNITUS;

EID: 16944362940     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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