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P05.01: Chromosomal microarray: beyond copy number variations
Author(s) -
Daum H.,
Meiner V.,
Zvi N.,
DraiHasid R.,
Yagel S.,
Yanai N.,
Zenvirt S.,
Frumkin A.
Publication year - 2018
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.19656
Subject(s) - uniparental disomy , copy number variation , snp array , genomic imprinting , medicine , amniocentesis , prenatal diagnosis , genetics , holoprosencephaly , snp , fetus , single nucleotide polymorphism , bioinformatics , chromosome , gene , biology , karyotype , pregnancy , dna methylation , genome , genotype , gene expression