Detection of chromosomal abnormalities, an outcome of ultrasound screening

Annals of the New York Academy of Sciences

Volumn 847, Issue , 1998, Pages 136-140

  Grandjean, Hélène ^a,b   Larroque, Danièle ^a,b   Levi, Salvator ^a,b   Team, The Eurofetus ^a,b  

^a Serv Univ Psychiat l'Enfant l'A   (France)

^b BRUGMANN UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; CONFERENCE PAPER; DIAGNOSTIC ACCURACY; DOWN SYNDROME; FEMALE; FETUS; FETUS DEATH; FETUS ECHOGRAPHY; FETUS KARYOTYPING; FETUS MALFORMATION; HUMAN; INDUCED ABORTION; MAJOR CLINICAL STUDY; PRENATAL DIAGNOSIS; TRISOMY 13; TRISOMY 18;

EID: 0031822747     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb08934.x     Document Type: Conference Paper

References (7)

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2. TWINNING, P. & J. ZUCCOLLO. 1993. The ultrasound markers of chromosomal disease: A retrospective study. Br. J. Radio). 66:408-114.
3. DEN HOLLANDER, N.S., T.E. COHEN OVERBEEK, R. HEYDANUS, P.A. STEWART, H. BRANDENBURG, F.L. Los, M.G. JAHODA & J.W. WLADIMIROFF. 1994. Cordocentesis for rapid karyotyping in fetuses with congenital anomalies or severe IUGR. Eur. J. Obstet. Gynecol. Reprod. Biol. 53:183-187.
4. MEAGHER, S., R. RENSHAW, A. SMITH & J. MILLIGAN. 1994. Chromosomal abnormalities detected after an abnormal ultrasound in pregnancy. Clin. Exp. Obstet. Gynecol. 21: 215-220.
5. CLAUSSEN, U., R. ULMER, E. BEINDER & H.J.L. VOIGT. 1994. Six years' experience with rapid karyotyping in prenatal diagnosis: Correlations between phenotype detected by ultrasound and fetal karyotype. Prenatal Diagn. 14:113-121.
6. NICOLAIDES, K.H., R.J. SNIJDERS, CM. GOSDEN, C. BERRY & S. CAMPBEL. 1992. Ultrasonographic markers of fetal chromosomal abnormalities. Lancet 340:704-707.
7. STOLL, C., B. DOTT, Y. ALEMBIK & M.P. ROTH. 1993. Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population. Hum. Genet. 91:37-41.