Two years' prospective experience using fluorescencein situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference15 articles.
1. PRENATAL DETECTION OF CHROMOSOME ANEUPLOIDIES BY FLUORESCENCE IN SITU HYBRIDIZATION: EXPERIENCE WITH 2000 UNCULTURED AMNIOTIC FLUID SAMPLES IN A PROSPECTIVE PRECLINICAL TRIAL
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. Prenatal diagnosis byin situ hybridization on uncultured amniocytes: Reduced sensitivity and potential risk of misdiagnosis in blood-stained samples
4. Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library
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. Desirable quality-control materials for the establishment of qualified external quality assessment on prenatal diagnosis of chromosomal aneuploidies;Clinica Chimica Acta;2018-12
2. Noninvasive Cell-Free DNA Prenatal Testing for Fetal Aneuploidy in Maternal Blood;Molecular Diagnostics;2017
3. FREE FETAL DNA AS A SCREENING TEST FOR ANEUPLOIDY – DOES IT ADD UP?;Fetal and Maternal Medicine Review;2014-11
4. Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis;Journal of Clinical Medicine;2014-07-24
5. Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases;CHINESE MED J-PEKING;2011
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