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Volumn 24, Issue 7, 2004, Pages 501-503

Unusual prenatal presentation of Beckwith-Wiedemann syndrome

Author keywords

Beckwith Wiedemann syndrome; Fetal hepatomegaly; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CLINICAL FEATURE; FEMALE; FETUS; HEPATOMEGALY; HUMAN; KIDNEY HYPERTROPHY; MACROGLOSSIA; PANCREAS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; UMBILICAL HERNIA;

EID: 4043057951     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.913     Document Type: Article
Times cited : (14)

References (7)
  • 1
    • 0036182963 scopus 로고    scopus 로고
    • Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects
    • DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP. 2002. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. Am J Hum Genet 70(3): 604-611.
    • (2002) Am J Hum Genet , vol.70 , Issue.3 , pp. 604-611
    • DeBaun, M.R.1    Niemitz, E.L.2    McNeil, D.E.3    Brandenburg, S.A.4    Lee, M.P.5    Feinberg, A.P.6
  • 2
    • 0029874214 scopus 로고    scopus 로고
    • Nonimmune fetal hydrops and placentomegaly: Diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH
    • Drut RM, Drut R. 1996. Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH. Am J Med Genet 62(2): 145-149.
    • (1996) Am J Med Genet , vol.62 , Issue.2 , pp. 145-149
    • Drut, R.M.1    Drut, R.2
  • 3
    • 4043152546 scopus 로고
    • Macroglossia and ankyloglossia in Beckwith-Wiedemann syndrome: Difficulties with prenatal diagnosis
    • Patterson GT, Ramasastry SS, Davis JU. 1988. macroglossia and ankyloglossia in Beckwith-Wiedemann syndrome: difficulties with prenatal diagnosis. Fetal Diagn Ther 9: 256-260.
    • (1988) Fetal Diagn Ther , vol.9 , pp. 256-260
    • Patterson, G.T.1    Ramasastry, S.S.2    Davis, J.U.3
  • 4
    • 0037154001 scopus 로고    scopus 로고
    • Wiedemann-Beckwith syndrome: Further prenatal characterization of the condition
    • Reish O, Lerer I, Amiel A, et al. 2002. Wiedemann-Beckwith syndrome: further prenatal characterization of the condition. Am J Med Genet 107(3): 209-213.
    • (2002) Am J Med Genet , vol.107 , Issue.3 , pp. 209-213
    • Reish, O.1    Lerer, I.2    Amiel, A.3
  • 5
    • 0025891267 scopus 로고
    • Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome
    • Viljoen DL, Jaquire Z, woods DL. 1991. Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome. Prenat Diagn 11: 167-175.
    • (1991) Prenat Diagn , vol.11 , pp. 167-175
    • Viljoen, D.L.1    Jaquire, Z.2    Woods, D.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.