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IEEE Transactions on Computational Imaging|January 16, 2016
Undersampled Phase Retrieval with OutliersDaniel S Weller, Ayelet Pnueli, Gilad Divon, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 11, 2004
Inferior vena cava thrombosis presenting as non-immune hydrops in the fetus of a woman with diabetesA Weissmann-Brenner, A Ferber, C O'Reilly-Green, et al.
European Journal of Pediatrics|November 1, 1985
Tetra-amelia with multiple malformations in six male fetuses of one kindredE Z Zimmer, E Taub, Y Sova, 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|November 20, 2009
The association of maternal BMI with fetal echogenic intracardiac foci and echogenic bowelEran Bornstein, Eyal Sheiner, Yoni Barnhard, et al.
Qualitative Health Research|November 17, 2022
More Than Just an Entertainment Show: Identification of Medical Clowns' Communication Skills and Therapeutic GoalsOrit Karnieli-Miller, Orna Divon-Ophir, Doron Sagi, et al.
ESMO Open|April 30, 2025
Refining prognostic tools for luminal breast cancer: genetic insights and comprehensive analysisL A Sinberger, T Zahavi, N Keren-Khadmy, et al.
American Journal of Obstetrics and Gynecology|August 10, 2010
Complete trisomy 21 vs translocation Down syndrome: a comparison of modes of ascertainmentEran Bornstein, Erez Lenchner, Alan Donnenfeld, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|July 2, 2015
The Effect of Maternal Obesity on Pregnancy Outcome in Correlation With Placental PathologyMichal Kovo, Elena Zion-Saukhanov, Letizia Schreiber, et al.
Cancer Management and Research|March 3, 2018
MicroRNA-mRNA expression profiles associated with medulloblastoma subgroup 4Sivan Gershanov, Helen Toledano, Shalom Michowiz, et al.
Translational Psychiatry|February 3, 2019
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approachElena Michaelovsky, Miri Carmel, Amos Frisch, et al.
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