메뉴 건너뛰기
Archives of Gynecology and Obstetrics
Volumn 274, Issue 4, 2006, Pages 243-245
Prenatal diagnosis of the 13q-syndrome through three-dimensional ultrasonography: A case report
Author keywords

Chromosomes 13; Deletion; Prenatal ultrasonography; Three dimensional imaging
Indexed keywords

ADULT; ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 13Q SYNDROME; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; FACE MALFORMATION; FEMALE; FETUS; FETUS ECHOGRAPHY; FINGER MALFORMATION; GASTROINTESTINAL MALFORMATION; GESTATION PERIOD; GROWTH RETARDATION; HOLOPROSENCEPHALY; HUMAN; KIDNEY MALFORMATION; LIP MALFORMATION; MENTAL DEFICIENCY; PRENATAL DIAGNOSIS; RARE DISEASE; RETINOBLASTOMA; THREE DIMENSIONAL IMAGING;
EID: 33745497512     PISSN: 09320067     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00404-006-0128-0     Document Type: Article
Times cited : (9)
References (8)
  • 1
    • 0028982746 scopus 로고
    • The 13q-syndrome: The molecular definition of a critical of deletion region in band 13q32
    • Brown S, Russo J, Chitayat D, Warburton D (1995) The 13q-syndrome: the molecular definition of a critical of deletion region in band 13q32. Am J Hum Genet 7:859-866
    • (1995) Am J Hum Genet , vol.7 , pp. 859-866
    • Brown, S.1    Russo, J.2    Chitayat, D.3    Warburton, D.4
  • 2
    • 0027402372 scopus 로고
    • Preliminary definition of a "critical region" of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature
    • Brown S, Gersen S, Anyane-Yeboa K, Warburton D (1993) Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature. Am J Med Genet 45(1):52-59
    • (1993) Am J Med Genet , vol.45 , Issue.1 , pp. 52-59
    • Brown, S.1    Gersen, S.2    Anyane-Yeboa, K.3    Warburton, D.4
  • 3
    • 0001481476 scopus 로고
    • Chromosome deletion in a case of retinoblastoma
    • Lele KP, Penrose LS, Stallard HB (1963) Chromosome deletion in a case of retinoblastoma. Ann Hum Genet 27:171-174
    • (1963) Ann Hum Genet , vol.27 , pp. 171-174
    • Lele, K.P.1    Penrose, L.S.2    Stallard, H.B.3
  • 5
    • 0035103327 scopus 로고    scopus 로고
    • Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
    • Chen CP, Chern SR, Lee CC, Chen WL, Wang W (2001) Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly. Prenat Diagn 21:102-105
    • (2001) Prenat Diagn , vol.21 , pp. 102-105
    • Chen, C.P.1    Chern, S.R.2    Lee, C.C.3    Chen, W.L.4    Wang, W.5
  • 6
    • 0031749316 scopus 로고    scopus 로고
    • 13q-in a fetus with ultrasonographic diagnosis of exencephaly in the first trimester
    • Lam YH, Tang MH, Ng LK (1998) 13q-in a fetus with ultrasonographic diagnosis of exencephaly in the first trimester. Prenat Diagn 18:634-635
    • (1998) Prenat Diagn , vol.18 , pp. 634-635
    • Lam, Y.H.1    Tang, M.H.2    Ng, L.K.3
  • 7
    • 17644423928 scopus 로고    scopus 로고
    • Prenatal diagnosis of 13q-syndrome in a fetus with Dandy-Walker malformation
    • Gul A, Cebeci A, Erol O, Ceylan Y, Basaran S, Yuksel A (2005) Prenatal diagnosis of 13q-syndrome in a fetus with Dandy-Walker malformation. Obstet Gynecol 105:1227-1229
    • (2005) Obstet Gynecol , vol.105 , pp. 1227-1229
    • Gul, A.1    Cebeci, A.2    Erol, O.3    Ceylan, Y.4    Basaran, S.5    Yuksel, A.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.