A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval

Clinical Genetics

Volumn 63, Issue 1, 2003, Pages 39-45

  DeWan, A T ^a   Parrado, A R ^a   Leal, Suzanne M ^a,b  

^a ROCKEFELLER UNIVERSITY   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Autosomal dominant non syndromic hearing loss (ADNSHL); DFNA20; DFNA26; Progressive hearing loss; USH1G

Indexed keywords

ALLELE; ARTICLE; AUDIOMETRY; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 17Q; CHROMOSOME MAP; CONTROLLED STUDY; FAMILY; GENE LOCUS; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; LINKAGE ANALYSIS; ONSET AGE; PRIORITY JOURNAL; STATISTICAL ANALYSIS; UNITED STATES; ADULT; AGED; CHROMOSOME 17; FEMALE; GENETICS; MALE; MIDDLE AGED; PEDIGREE;

ADULT; AGED; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; DEAFNESS; FEMALE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIDDLE AGED; PEDIGREE;

EID: 0038755204     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2003.630106.x     Document Type: Article

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