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OP22.08: Integrating ultrasound findings with chromosomal microarray stretches of homozygosity and principles in founder populations
Author(s) -
Daum H.,
Lerer I.,
Frumkin A.,
Rosenak D.,
Yanai N.,
Yagel S.,
Meiner V.
Publication year - 2017
Publication title -
ultrasound in obstetrics and gynecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.202
H-Index - 141
eISSN - 1469-0705
pISSN - 0960-7692
DOI - 10.1002/uog.17905
Subject(s) - runs of homozygosity , disease gene identification , genetics , snp array , amniocentesis , founder effect , prenatal diagnosis , consanguinity , copy number variation , medicine , snp , chorionic villus sampling , snp genotyping , mutation , biology , gene , exome sequencing , single nucleotide polymorphism , fetus , genome , haplotype , pregnancy , allele , genotype
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