Fluorescencein situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference29 articles.
1. New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report.
2. Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells
3. Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactivein situ hybridization
4. An embryogenic model to explain cytogenetic inconsistencies observed in chorionic villus versus fetal tissue
5. Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84
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1. Application of fluorescence in situ hybridization (FISH) as a tool to aid cytogenetics in 1,409 fetal samples;Clinical and Experimental Obstetrics & Gynecology;2016-10-10
2. Molecular Cytogenetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2015-11-23
3. Molecular Cytogenetics and Prenatal Diagnosis;Genetic Disorders and the Fetus;2010-09-24
4. Cytogenetics in reproductive medicine: The contribution of comparative genomic hybridization (CGH);BioEssays;2003-02-20
5. FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy;Prenatal Diagnosis;2001
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