Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p

Genomics

Volumn 41, Issue 1, 1997, Pages 70-74

  Van Camp, Guy ^a   Coucke, Paul J ^a   Kunst, Hendrik ^b   Schatteman, Isabelle ^a   Van Velzen, Désirée ^a   Marres, Henri ^b   Van Ewijk, Marleen ^b   Declau, Frank ^a   Van Hauwe, Peter ^a   Meyers, Johan ^a   Kenyon, Judy ^e   Smith, Shelley D ^e   Smith, Richard J H ^c   Djelantik, Bulantrisna ^d   Cremers, Cor W R J ^b   Van De Heyning, Paul H ^a   Willems, Patrick J ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

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

^d PADJADJARAN UNIVERSITY   (Indonesia)

^e NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BELGIUM; CHROMOSOME 1P; GENE MAPPING; GENETIC LINKAGE; HAPLOTYPE; HEARING LOSS; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MULTIGENE FAMILY; NETHERLANDS; PRIORITY JOURNAL; UNITED STATES;

EID: 0031127215     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4624     Document Type: Article

References (13)

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