A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

Human Molecular Genetics

Volumn 5, Issue 7, 1996, Pages 1047-1050

  Manolis, Evangelos N ^a   Yandavi, Naidu ^b,c,d   Nadol Jr , Joseph B ^a   Eavey, Roland D ^a   McKenna, Michael ^a   Rosenbaum, Stella ^b   Khetarpal, Uman ^a,e   Halpin, Christopher ^a   Merchant, Saumil N ^a   Duyk, Geoffrey M ^b,f   MacRae, Calum ^b   Seidman, Christine E ^c   Seidman, J G ^b  

^a HARVARD MEDICAL SCHOOL   (United States)

^b HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

^d Medical School   (United States)

^e SUNY UPSTATE MEDICAL UNIVERSITY   (United States)

^f MILLENNIUM PHARMACEUTICALS INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA MARKER;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 14Q; CLINICAL ARTICLE; DNA POLYMORPHISM; DNA RECOMBINATION; FEMALE; GENE MAPPING; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; ONSET AGE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; TANDEM REPEAT;

ADULT; AGE OF ONSET; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 14; FEMALE; GENES, DOMINANT; HAPLOTYPES; HEARING LOSS, SENSORINEURAL; HUMANS; LOD SCORE; LYMPHOCYTES; MALE; MIDDLE AGED; PEDIGREE;

EID: 8944247751     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.7.1047     Document Type: Article

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