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Volumn 25, Issue 6, 2005, Pages 629-630

Prenatal sonographic appearance of cryptophthalmos in Fraser syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE MALFORMATION; CASE REPORT; CLEFT LIP; CLEFT PALATE; CLINICAL FEATURE; CRYPTOPHTHALMOS; EAR MALFORMATION; EYE MALFORMATION; FEMALE; FETUS; FRASER SYNDROME; GENITAL MALFORMATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; KIDNEY AGENESIS; LARYNX STENOSIS; MENTAL DEFICIENCY; NOSE MALFORMATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SYNDACTYLY; UMBILICAL HERNIA;

EID: 20644465614     PISSN: 09607692     EISSN: None     Source Type: Journal    
DOI: 10.1002/uog.1905     Document Type: Article
Times cited : (13)

References (12)
  • 2
    • 0023242382 scopus 로고
    • The clinical spectrum of the Fraser syndrome: Report of three new cases and review
    • Gattuso J, Patron MA, Baraitser M. The clinical spectrum of the Fraser syndrome: report of three new cases and review. J Med Genet 1987; 24: 549-555.
    • (1987) J Med Genet , vol.24 , pp. 549-555
    • Gattuso, J.1    Patron, M.A.2    Baraitser, M.3
  • 4
    • 0025058360 scopus 로고
    • Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn
    • Ramsing M, Rehder H, Holzgreve W, Meinecke P, Lenz W. Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn. Clin Genet 1990; 37: 84-96.
    • (1990) Clin Genet , vol.37 , pp. 84-96
    • Ramsing, M.1    Rehder, H.2    Holzgreve, W.3    Meinecke, P.4    Lenz, W.5
  • 8
    • 0023767119 scopus 로고
    • Fraser syndrome (cryptophthalmos-syndactyly syndrome): A review of eleven cases with postmortem findings
    • Boyd PA, Keeling JW, Lindenbaum RH. Fraser syndrome (cryptophthalmos- syndactyly syndrome): a review of eleven cases with postmortem findings. Am J Med Genet 1988; 31: 159-168.
    • (1988) Am J Med Genet , vol.31 , pp. 159-168
    • Boyd, P.A.1    Keeling, J.W.2    Lindenbaum, R.H.3
  • 9
    • 0024643926 scopus 로고
    • Fraser syndrome: Prenatal ultrasonic detection
    • Serville F, Carles D, Broussin B. Fraser syndrome: prenatal ultrasonic detection. Am J Med Genet 1989; 32: 561-563.
    • (1989) Am J Med Genet , vol.32 , pp. 561-563
    • Serville, F.1    Carles, D.2    Broussin, B.3
  • 11
    • 1042278816 scopus 로고    scopus 로고
    • Prospective prenatal diagnosis of Fraser syndrome variant in a family with negative history
    • Maruotti GM, Paladini D, Agangi A, Martinelli P. Prospective prenatal diagnosis of Fraser syndrome variant in a family with negative history. Prenat Diagn 2004; 24: 69-70.
    • (2004) Prenat Diagn , vol.24 , pp. 69-70
    • Maruotti, G.M.1    Paladini, D.2    Agangi, A.3    Martinelli, P.4
  • 12
    • 0025186104 scopus 로고
    • Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks
    • Schauer GM, Dunn LK, Godmilow L, Eagle RC Jr, Knisely AS. Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks. Am J Med Genet 1990; 37: 583-591.
    • (1990) Am J Med Genet , vol.37 , pp. 583-591
    • Schauer, G.M.1    Dunn, L.K.2    Godmilow, L.3    Eagle Jr., R.C.4    Knisely, A.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.