Fluorescence in situ hybridization of chorionic interphase cells for prenatal screening of Down syndrome

European Journal of Obstetrics Gynecology and Reproductive Biology

Volumn 94, Issue 1, 2001, Pages 46-50

  Tóth, András ^a   Tardy, Erika P ^a   Hajdu, Krisztina ^a   Bátorfi, József ^a   Doszpod, József ^a   Egyed, Jenõ ^a   Gáti, István ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

Author keywords

Chorionic villi; Down syndrome; Fluorescence in situ hybridization; Prenatal screening

Indexed keywords

ADULT; ARTICLE; CHORION VILLUS; CHROMOSOME ANALYSIS; CONTROLLED STUDY; CYTOGENETICS; DIAGNOSTIC ACCURACY; DOWN SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTERPHASE; PRENATAL DIAGNOSIS; PRENATAL SCREENING; PRIORITY JOURNAL; RELIABILITY; SCREENING TEST;

EID: 0035178734     PISSN: 03012115     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0301-2115(00)00310-9     Document Type: Article

References (20)

1. Molecular cytogenetics: An essential component of modern prenatal diagnosis
2. Detection of aneuploidy involving chromosomes 13, 18, or 21 by fluorescence in situ hybridization to interphase and metaphase amniocytes
3. Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)
4. Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study
5. Prenatal detection of chromsome aneuploidies by fluorescence in situ hybridization: Experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial
6. Defining the role of fluorescence in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies
7. A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis
8. Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy
9. Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH
10. Why confine chorionic villus (placental) biopsy to the first trimester?
11. Benefits of placental biopsies for rapid karyotyping in the second and third trimesters (late chorionic villus sampling) in high-risk pregnancies
12. A prospective comparative study on transabdominal chorionic villus sampling and amniocentesis performed at 10-13 weeks gestation
13. Accuracy of cytogenetic findings on chorionic villus sampling (CVS) diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centers contributing to EUCROMIC 1986-1992
14. Fluorescent in situ hybridization (FISH): A new application in the delineation of true vs. Pseudomosaicism in prenatal diagnosis
15. Rapid prenatal diagnosis by fluorescent in situ hybridization of chorionic villi: An adjunct to long-term culture and karyotype
16. Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization
17. Cross-hybridization of the chromosme 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by FISH
18. Cross-hybridization of the chromosome 13/21 alpha satellite DNA to chromosome 22 or a rare polymorphysm
19. YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome
20. Preanatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization