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Volumn 132 A, Issue 2, 2005, Pages 215-218

Familial hyper- and hypopigmentation with age-related pattern change [3]

Author keywords

[No Author keywords available]

Indexed keywords

AGING; ANAMNESIS; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL FEATURE; FAMILY; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; LETTER; NEUROFIBROMATOSIS; NEWBORN PERIOD; PEDIGREE; PRIORITY JOURNAL;

EID: 11844266554     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30381     Document Type: Letter
Times cited : (8)

References (9)
  • 3
    • 0042160192 scopus 로고    scopus 로고
    • Familial cutis tricolor: A possible example of paradominant inheritance
    • Baba M, Seckin D, Akcali C, Happle R. 2003. Familial cutis tricolor: A possible example of paradominant inheritance. Eur J Dermatol 13:343-345.
    • (2003) Eur J Dermatol , vol.13 , pp. 343-345
    • Baba, M.1    Seckin, D.2    Akcali, C.3    Happle, R.4
  • 5
    • 0027526289 scopus 로고
    • Autosomal dominant multiple cafe-au-lait spots and neurofibromatosis-1: Evidence of non-linkage
    • Charrow J, Listernick R, Ward K. 1993. Autosomal dominant multiple cafe-au-lait spots and neurofibromatosis-1: Evidence of non-linkage. Am J Med Genet 45:606-608.
    • (1993) Am J Med Genet , vol.45 , pp. 606-608
    • Charrow, J.1    Listernick, R.2    Ward, K.3
  • 6
    • 0030788743 scopus 로고    scopus 로고
    • "Cutis tricolor": Congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: An unusual example of twin spotting?
    • Happle R, Barbi G, Eckert D, Kennerknecht I. 1997. "Cutis tricolor": Congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: An unusual example of twin spotting? J Med Genet 34:676-678.
    • (1997) J Med Genet , vol.34 , pp. 676-678
    • Happle, R.1    Barbi, G.2    Eckert, D.3    Kennerknecht, I.4
  • 9
    • 0037081077 scopus 로고    scopus 로고
    • A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple cafe-au-lait spots
    • Whiteside D, McLeod R, Graham G, Steckley JL, Booth K, Somerville MJ, Andrew SE. 2002. A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple cafe-au-lait spots. Cancer Res 62:359-362.
    • (2002) Cancer Res , vol.62 , pp. 359-362
    • Whiteside, D.1    McLeod, R.2    Graham, G.3    Steckley, J.L.4    Booth, K.5    Somerville, M.J.6    Andrew, S.E.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.