Sarit Kahana

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

Lena Sagi‐Dain, Lital Cohen Vig, Sarit Kahana et al. · Genetics in Medicine · 2019 · 66 citations · Full text

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations

Idit Maya, Reuven Sharony, Shiri Yacobson et al. · Genetics in Medicine · 2017 · 61 citations · Full text

Reproductive Genetic Counseling, Counseling, Genetic Testing +8

Cut‐off value of nuchal translucency as indication for chromosomal microarray analysis

Idit Maya, Shiri Yacobson, Sarit Kahana et al. · Ultrasound in Obstetrics and Gynecology · 2017 · 60 citations · Full text

A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis

Aviva Mimouni-Bloch, Josepha Yeshaya, Sarit Kahana et al. · European Journal of Paediatric Neurology · 2015 · 52 citations

Genetic Disorder, 2P16.1-p15 Microdeletion Syndrome, Genetics +7

Chromosomal microarray analysis in fetuses with aberrant right subclavian artery

Idit Maya, Sarit Kahana, Josepha Yeshaya et al. · Ultrasound in Obstetrics and Gynecology · 2016 · 45 citations · Full text