Single‐nucleotide Polymorphism‐based Chromosomal Microarray Analysis Provides Clues and Insights into Disease Mechanisms
ULTRASOUND IN OBSTETRICS & GYNECOLOGY（2019）
Key words
absence of heterozygosity,biochemical screening test,CMA,fetal malformation,imprinting disorder,Kagami-Ogata syndrome,maternal serum analyte,monogenic disease,prenatal diagnosis,runs of homozygosity,uniparental disomy
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