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Volumn 129, Issue 11, 2009, Pages 2628-2636

Erratum: Phenotypic and genotypic analyses of genetic skin disease through the online mendelian inheritance in man (OMIM) database (Journal of Investigative Dermatology (2009) 129 (2628-2636) DOI:10.1038/jid.2009.108);Phenotypic and genotypic analyses of genetic skin disease through the online mendelian inheritance in man (OMIM) database

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Indexed keywords

PROTEIN;

EID: 70350068764     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/jid.2009.363     Document Type: Erratum
Times cited : (54)

References (9)
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    • Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: Genetic relationship to ataxia telangiectasia
    • Jaspers NG, Taalman RD, Baan C (1988) Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia. Am J Hum Genet 42:66-73
    • (1988) Am J Hum Genet , vol.42 , pp. 66-73
    • Jaspers, N.G.1    Taalman, R.D.2    Baan, C.3
  • 8
    • 0036247733 scopus 로고    scopus 로고
    • Connexin mutations in hearing loss, dermatological and neurological disorders
    • Rabionet R, Lopez-Bigas N, Arbones ML, Estivill X (2002) Connexin mutations in hearing loss, dermatological and neurological disorders. Trends Mol Med 8:205-212
    • (2002) Trends Mol Med , vol.8 , pp. 205-212
    • Rabionet, R.1    Lopez-Bigas, N.2    Arbones, M.L.3    Estivill, X.4
  • 9
    • 0020619254 scopus 로고
    • Bloom's syndrome: Evidence for an increased mutation frequency in vivo
    • Vijayalaxmi, Evans HJ, Ray JH, German J (1983) Bloom's syndrome: evidence for an increased mutation frequency in vivo. Science 221:851-853
    • (1983) Science , vol.221 , pp. 851-853
    • Vijayalaxmi1    Evans, H.J.2    Ray, J.H.3    German, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.