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Volumn 68, Issue 1, 2001, Pages 254-260

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12Q; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; HAPLOTYPE; HEARING IMPAIRMENT; HUMAN; PEDIGREE; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0035168047     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/316925     Document Type: Article
Times cited : (51)

References (25)
  • 4
    • 0033911995 scopus 로고    scopus 로고
    • Phenotypes of patients with "simple" Mendelian disorders are complex traits: Thresholds, modifiers, and systems dynamics
    • (2000) Am J Hum Genet , vol.66 , pp. 1729-1735
    • Dipple, K.M.1    McCabe, E.R.B.2
  • 9
    • 4244079632 scopus 로고
    • Genetic hearing loss with no associated abnormalities
    • Konigsmark BW, Gorlin RJ (eds) Genetic and metabolic deafness. W. B. Saunders Co., Philadelphia
    • (1976) , pp. 7-23
    • Konigsmark, B.W.1    Gorlin, R.J.2
  • 18
    • 0023880559 scopus 로고
    • Threshold of hearing as a function of age and sex for the typical unscreened population
    • (1988) Br J Audiol , vol.22 , pp. 5-20
    • Robinson, D.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.