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Yuval Yaron

Showing results (81-90 of 122) with videos related to

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European Journal of Medical Genetics|August 24, 2025
Overview and expansion of CEP85L-associated lissencephalyIsabell Schumann, Rami Abou Jamra, Robin-Tobias Jauss, et al.
American Journal of Obstetrics & Gynecology MFM|June 13, 2023
Diagnostic yield with exome sequencing in prenatal severe bilateral ventriculomegaly: a systematic review and meta-analysisHiba J Mustafa, Enaja V Sambatur, Julie P Barbera, et al.
Human Reproduction (Oxford, England)|May 10, 2020
Maternal plasma genome-wide cell-free DNA can detect fetal aneuploidy in early and recurrent pregnancy loss and can be used to direct further workupYuval Yaron, Montse Pauta, Celia Badenas, et al.
Journal of Assisted Reproduction and Genetics|December 1, 2004
Prospective randomized comparison of two embryo culture systems: P1 medium by Irvine Scientific and the Cook IVF MediumDalit Ben-Yosef, Ami Amit, Foad Azem, et al.
European Journal of Medical Genetics|January 18, 2019
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providersAlexandra Benachi, Jessica Caffrey, Pavel Calda, et al.
Fetal Diagnosis and Therapy|February 7, 2004
Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophyMira Malcov, Tamar Schwartz, Nava Mei-Raz, et al.
Prenatal Diagnosis|February 19, 2026
Exome Sequencing in Prenatally Diagnosed Isolated Neural Tube Defects: A Subtype-Specific AnalysisAdi Botvinik, Vered Offen Glasner, Adi Reches, et al.
Journal of Neuromuscular Diseases|February 20, 2025
A rare homozygous <i>CAPN3</i> variant with distinct clinical features in unrelated families of Iraqi Jewish descentNurit Assia Batzir, Naama Orenstein, Yuval Yaron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutationNoam Domniz, Liat Ries Levavi, Michal Berkenstadt, et al.
Cell Stem Cell|March 29, 2008
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryosRachel Eiges, Achia Urbach, Mira Malcov, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
European Journal of Medical Genetics|August 24, 2025
Overview and expansion of CEP85L-associated lissencephalyIsabell Schumann, Rami Abou Jamra, Robin-Tobias Jauss, et al.
American Journal of Obstetrics & Gynecology MFM|June 13, 2023
Diagnostic yield with exome sequencing in prenatal severe bilateral ventriculomegaly: a systematic review and meta-analysisHiba J Mustafa, Enaja V Sambatur, Julie P Barbera, et al.
Human Reproduction (Oxford, England)|May 10, 2020
Maternal plasma genome-wide cell-free DNA can detect fetal aneuploidy in early and recurrent pregnancy loss and can be used to direct further workupYuval Yaron, Montse Pauta, Celia Badenas, et al.
Journal of Assisted Reproduction and Genetics|December 1, 2004
Prospective randomized comparison of two embryo culture systems: P1 medium by Irvine Scientific and the Cook IVF MediumDalit Ben-Yosef, Ami Amit, Foad Azem, et al.
European Journal of Medical Genetics|January 18, 2019
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providersAlexandra Benachi, Jessica Caffrey, Pavel Calda, et al.
Fetal Diagnosis and Therapy|February 7, 2004
Multiplex nested PCR for preimplantation genetic diagnosis of spinal muscular atrophyMira Malcov, Tamar Schwartz, Nava Mei-Raz, et al.
Prenatal Diagnosis|February 19, 2026
Exome Sequencing in Prenatally Diagnosed Isolated Neural Tube Defects: A Subtype-Specific AnalysisAdi Botvinik, Vered Offen Glasner, Adi Reches, et al.
Journal of Neuromuscular Diseases|February 20, 2025
A rare homozygous <i>CAPN3</i> variant with distinct clinical features in unrelated families of Iraqi Jewish descentNurit Assia Batzir, Naama Orenstein, Yuval Yaron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutationNoam Domniz, Liat Ries Levavi, Michal Berkenstadt, et al.
Cell Stem Cell|March 29, 2008
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryosRachel Eiges, Achia Urbach, Mira Malcov, et al.
Pageof 13