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Volumn 21, Issue 2, 2003, Pages 146-150

The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research

Author keywords

Database; DNA bank; Genetic; Iranian; Mutation bank; Polymorphism

Indexed keywords

DNA;

EID: 0037262315     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10164     Document Type: Article
Times cited : (26)

References (18)
  • 2
    • 0032969992 scopus 로고    scopus 로고
    • Genomics and hearing impairment
    • Keats BJB, Berlin CI. 1999. Genomics and hearing impairment. Genome Res 9:7-16.
    • (1999) Genome Res , vol.9 , pp. 7-16
    • Keats, B.J.B.1    Berlin, C.I.2
  • 14
    • 0033812813 scopus 로고    scopus 로고
    • Connexin 26 mutations associated with nonsyndromic hearing loss
    • Park HJ, Hahn SH, Chun YM, Park K, Kim HN. 2000. Connexin 26 mutations associated with nonsyndromic hearing loss. Laryngoscope 110:1535-1538.
    • (2000) Laryngoscope , vol.110 , pp. 1535-1538
    • Park, H.J.1    Hahn, S.H.2    Chun, Y.M.3    Park, K.4    Kim, H.N.5
  • 15
    • 0026663506 scopus 로고
    • Genetic deafness
    • Reardon W. 1992. Genetic deafness. J Med Genet 29:521-526.
    • (1992) J Med Genet , vol.29 , pp. 521-526
    • Reardon, W.1
  • 16
    • 0030946546 scopus 로고    scopus 로고
    • Nonsyndromic hearing impairment: Unparalleled heterogeneity
    • Van Camp G, Willems PJ, Smith RJH. 1997. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 60:758-764.
    • (1997) Am J Hum Genet , vol.60 , pp. 758-764
    • Van Camp, G.1    Willems, P.J.2    Smith, R.J.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.