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Volumn 68, Issue 2, 2001, Pages 495-500

A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BELGIUM; CHROMOSOME 15; CHROMOSOME 7Q; CHROMOSOME MAP; CLINICAL ARTICLE; COCHLEA; CONDUCTION DEAFNESS; FAMILY STUDY; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; MIDDLE EAR; OTOSCLEROSIS; PENETRANCE; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0035121870     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318185     Document Type: Article
Times cited : (92)

References (26)
  • 7
    • 0002491507 scopus 로고    scopus 로고
    • Otosclerosis
    • Martini A, Read A, Stephens D (eds) Genetics and hearing impairment. Whurr, London
    • (1996) , pp. 221-230
    • Declau, F.1    Van de Heyning, P.2
  • 10
    • 0031446469 scopus 로고    scopus 로고
    • Effect of retinoic acid on otic capsule chondrogenesis in high-density culture suggests disruption of epithelial-mesenchymal interactions
    • (1997) Teratology , vol.56 , pp. 233-240
    • Frenz, D.A.1    Liu, W.2
  • 16
    • 0001505845 scopus 로고
    • Genetic problems in otosclerosis
    • Schuknecht HF (ed) Otosclerosis. Little Brown, Boston
    • (1962) , pp. 109-117
    • Larsson, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.