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Article

Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test

22 Jan 2014

Abstract excerpt

OBJECTIVE: The aim of this study was to assess the detection of chromosomal mosaicism in chorionic villus (CVS) and amniotic fluid (AF) samples using array comparative genomic hybridization (aCGH) and quantitative fluorescent polymerase chain reaction. METHODS: All patients undergoing invasive prenatal testing by aCGH at a specialist prenatal screening service were included in the study. A total of 1609 samples...

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Share to Genetic Syndromes and Imprinting
Share to Genomic variations and chromosomal abnormalities
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PMID: 24453008
DOI: 10.1002/pd.4332

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