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Volumn 115, Issue 4, 2000, Pages 664-667

Assignment of the gene for a new hereditary nail disorder, isolated congenital nail dysplasia, to chromosome 17p13

Author keywords

Chromosome I7pl3; Isolated congenital nail dysplasia

Indexed keywords

DNA;

EID: 0033770363     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1747.2000.00102.x     Document Type: Article
Times cited : (16)

References (36)
  • 13
    • 0032965997 scopus 로고    scopus 로고
    • Human keratin diseases: The increasing spectrum of disease and subtlety of the phenotype-genotype correlation
    • (1999) Br J Dermatol , vol.140 , pp. 815-828
    • Irvine, A.D.1    McLean, W.H.2
  • 15
    • 0012920802 scopus 로고    scopus 로고
    • Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: Implications for protein structure and clinical phenotype
    • (1999) J Invest Dermatol , vol.113 , pp. 607-612
    • Korge, B.P.1    Hamm, H.2    Jury, C.S.3
  • 25
    • 0032877634 scopus 로고    scopus 로고
    • ATP2A2 mutations in Darier's disease: Variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class
    • (1999) Hum Mol Genet , vol.8 , pp. 1621-1630
    • Ruiz-Perez, V.L.1    Carter, S.A.2    Healy, E.3
  • 29
    • 0002725696 scopus 로고
    • Developmental abnormalities
    • Samman PD, Fenton DA (eds.). Samman's The Nails in Diseases, 5th edn. Oxford: Butterworth Heinemann
    • (1995) , pp. 183-208
    • Samman, P.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.