Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish-Reference-Cited by-同舟云学术

Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish

Published:1995-09 Issue:9 Volume:15 Page:831-834
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Verlinsky Y.,Ginsberg N.,Chmura M.,Freidine M.,White M.,Strom C.,Kuliev A.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference7 articles.

1. Fluorescencein situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells

2. Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescencein situ hybridization

3. Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescencein situ hybridization

4. (1989). Heterochromatic Regions of chromosomes, Moscow: Nauka (in Russian).

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