Single-nucleotide polymorphism-based chromosomal microarray analysis provides clues and insights into disease mechanisms.

Hagit DaumV MeinerN HacohenN ZviA EilatR Drai-HasidSimcha YagelS ZenvirtA Frumkin

Published in: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology (2020)

Prenatal CMA, based on oligo and SNP platforms, increases the diagnostic yield and enables a wider spectrum of disorders to be detected through the identification of complex genetic etiologies beyond only copy number variants. Copyright © 2019 ISUOG. Published by John Wiley & Sons Ltd.

Keyphrases

copy number
genome wide
mitochondrial dna
dna methylation
pregnant women
bioinformatics analysis
systematic review