Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: Clinical and genetic implications

American Journal of Human Genetics

Volumn 66, Issue 5, 2000, Pages 1715-1720

  Kumar, Shrawan ^a   Deffenbacher, Karen ^a   Marres, Henri A M ^b   Cremers, Cor W R J ^b   Kimberling, William J ^a  

^a BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRANCHIOOTORENAL SYNDROME; CHROMOSOME 1Q; FEMALE; GENE; GENETIC LINKAGE; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0033942027     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302890     Document Type: Article

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