A pathogenic variant in the uncharacterized RNF212B gene results in severe aneuploidy male infertility and repeated IVF failure by Gershoni, Moran, Braun, Tslil, Hauser, Ron, Barda, Shimi, Lehavi, Ofer, Malcov, Mira, Frumkin, Tsvia, Kalma, Yael, Pietrokovski, Shmuel, Arama, Eli, Kleiman, Sandra E.

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Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype by Malcov, Mira, Gold, Veronica, Peleg, Sagit, Frumkin, Tsvia, Azem, Foad, Amit, Ami, Ben-Yosef, Dalit, Yaron, Yuval, Reches, Adi, Barda, Shimi, Kleiman, Sandra E, Yogev, Leah, Hauser, Ron

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Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations by Amir, Hadar, Barbash-Hazan, Shiri, Kalma, Yael, Frumkin, Tsvia, Malcov, Mira, Samara, Nivin, Hasson, Joseph, Reches, Adi, Azem, Foad, Ben-Yosef, Dalit

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Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos by Eiges, Rachel, Urbach, Achia, Malcov, Mira, Frumkin, Tsvia, Schwartz, Tamar, Amit, Ami, Yaron, Yuval, Eden, Amir, Yanuka, Ofra, Benvenisty, Nissim, Ben-Yosef, Dalit

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Obstetric and neonatal outcomes of pregnancies conceived after preimplantation genetic diagnosis: cohort study and meta-analysis by Hasson, Joseph, Limoni, Dana, Malcov, Mira, Frumkin, Tsvia, Amir, Hadar, Shavit, Tal, Bay, BjØrn, Many, Ariel, Almog, Benjamin

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Time-lapse imaging reveals delayed development of embryos carrying unbalanced chromosomal translocations by Amir, Hadar, Barbash-Hazan, Shiri, Kalma, Yael, Frumkin, Tsvia, Malcov, Mira, Samara, Nivin, Hasson, Joseph, Reches, Adi, Azem, Foad, Ben-Yosef, Dalit

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Complex chromosomal rearrangement—a lesson learned from PGS by Frumkin, Tsvia, Peleg, Sagit, Gold, Veronica, Reches, Adi, Asaf, Shiri, Azem, Foad, Ben-Yosef, Dalit, Malcov, Mira

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Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysis by Frumkin, Tsvia, Malcov, Mira, Yaron, Yuval, Ben-Yosef, Dalit

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Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos by Eiges, Rachel, Urbach, Achia, Malcov, Mira, Frumkin, Tsvia, Schwartz, Tamar, Amit, Ami, Yaron, Yuval, Eden, Amir, Yanuka, Ofra, Benvenisty, Nissim, Ben-Yosef, Dalit

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Human embryonic stem cells carrying mutations for severe genetic disorders by Frumkin, Tsvia, Malcov, Mira, Telias, Michael, Gold, Veronica, Schwartz, Tamar, Azem, Foad, Amit, Ami, Yaron, Yuval, Ben-Yosef, Dalit

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