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Volumn 133, Issue 5 I, 2006, Pages 445-447

Familial case of Parkes-Weber syndrome;Syndrome de Parkes-Weber familial

Author keywords

[No Author keywords available]

Indexed keywords

AMENORRHEA; ANGIOMA; ANGIOOSTEOHYPERTROPHY SYNDROME; ARTICLE; CASE REPORT; CLINICAL FEATURE; COLOR ULTRASOUND FLOWMETRY; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC TEST; EXTRACHROMOSOMAL INHERITANCE; FAMILIAL DISEASE; FEMORAL ARTERY FLOW; HUMAN; LEG; MALE; NEWBORN; VEIN DILATATION;

EID: 33747704295     PISSN: 01519638     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0151-9638(06)70936-x     Document Type: Article
Times cited : (17)

References (8)
  • 1
    • 0028900599 scopus 로고
    • Familial Klippel Trenaunay syndrome: A case report
    • Graven N, Wright AL. Familial Klippel Trenaunay syndrome: a case report. Clin Exp Dermatol 1995;20:76-9.
    • (1995) Clin Exp Dermatol , vol.20 , pp. 76-79
    • Graven, N.1    Wright, A.L.2
  • 3
    • 0034640654 scopus 로고    scopus 로고
    • Klippel-Trenaunay syndrome
    • Cohen MM Jr. Klippel-Trenaunay syndrome. Am J Med Genet 2000;93:171-5.
    • (2000) Am J Med Genet , vol.93 , pp. 171-175
    • Cohen Jr., M.M.1
  • 4
    • 0026778316 scopus 로고
    • Genetic aspects of the Klippel-Trenaunay syndrome
    • Alvoet GE, Jorens PG, Roelen LM. Genetic aspects of the Klippel-Trenaunay syndrome: Br J Dermatol 1992;126:603-7.
    • (1992) Br J Dermatol , vol.126 , pp. 603-607
    • Alvoet, G.E.1    Jorens, P.G.2    Roelen, L.M.3
  • 5
    • 0031800996 scopus 로고    scopus 로고
    • Familial segregation of hemangiomas and vascular malformations. Malformations as an autosomal dominant trait
    • Blei F, Walter J, Orlow SJ, Marchut DA. Familial segregation of hemangiomas and vascular malformations. Malformations as an autosomal dominant trait. Arch Dermatol 1998;134:718-22.
    • (1998) Arch Dermatol , vol.134 , pp. 718-722
    • Blei, F.1    Walter, J.2    Orlow, S.J.3    Marchut, D.A.4
  • 6
    • 0032801893 scopus 로고    scopus 로고
    • Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes
    • Steijlen PM, Van Steensen MA. Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes. Am J Med Genet 1999;85:359-60.
    • (1999) Am J Med Genet , vol.85 , pp. 359-360
    • Steijlen, P.M.1    Van Steensen, M.A.2
  • 8
    • 0347362524 scopus 로고    scopus 로고
    • Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations
    • Eerola I, Boon LM, Mulliken JB, Burrows PE, Dompmartin A, Watanabe S, et al. Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutations. Am J Hum Genet 2003;73:1240-9.
    • (2003) Am J Hum Genet , vol.73 , pp. 1240-1249
    • Eerola, I.1    Boon, L.M.2    Mulliken, J.B.3    Burrows, P.E.4    Dompmartin, A.5    Watanabe, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.