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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 13, 2017
The yield of the prenatal work-up in intrauterine growth restriction and the spectrum of fetal abnormalities detected postnatally <sup>†</sup>Rivka Sukenik-Halevy, Adi Katz, Rivka H Regev, et al.
Virchows Archiv : an International Journal of Pathology|November 18, 2015
Agenesis of the corpus callosum. An autopsy study in fetusesDebora Kidron, Daniel Shapira, Liat Ben Sira, et al.
Early Human Development|December 21, 2010
TERC telomerase subunit gene copy number in placentas from pregnancies complicated with intrauterine growth restrictionTal Biron-Shental, Dvora Kidron, Rivka Sukenik-Halevy, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|February 2, 2018
The association between maternal serum first trimester free βhCG, second trimester intact hCG levels and foetal growth restriction and preeclampsiaReuven Sharony, Maya Sharon-Weiner, Debora Kidron, et al.
Ophthalmic Genetics|April 21, 2018
Ophthalmic manifestations of Heimler syndrome due to PEX6 mutationsNutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, et al.
Cancer Genetics and Cytogenetics|October 20, 2009
Telomere aggregate formation in placenta specimens of pregnancies complicated with pre-eclampsiaRivka Sukenik-Halevy, Moshe Fejgin, Devora Kidron, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|February 20, 2018
Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literatureLena Sagi-Dain, Amihood Singer, Yarin Hadid, et al.
Genetic Testing|May 3, 2008
Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi JewsNoa Auslender, Dikla Bandah, Leah Rizel, et al.
European Journal of Medical Genetics|July 24, 2020
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndromeIdit Maya, Sarit Kahana, Ifaat Agmon-Fishman, et al.
Journal of Perinatal Medicine|May 30, 2018
Chromosomal microarray findings in pregnancies with an isolated pelvic kidneyLena Sagi-Dain, Amihood Singer, Ayala Frumkin, et al.
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