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Adi Reches

Showing results (11-20 of 45) with videos related to

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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|March 8, 2018
The genetic and clinical outcome of isolated fetal muscular ventricular septal defect (VSD)Ran Svirsky, Dana Brabbing-Goldstein, Uri Rozovski, et al.
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
Plos One|March 16, 2022
NK-92 cells retain vitality and functionality when grown in standard cell culture conditionsRebecca Kotzur, Alexandra Duev-Cohen, Inbal Kol, et al.
Fertility and Sterility|May 11, 2020
Bypassing physiological puberty, a novel procedure of oocyte cryopreservation at age 7: a case report and review of the literatureFoad Azem, Avivit Brener, Gustavo Malinger, et al.
Prenatal Diagnosis|April 25, 2007
Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended familyAdi Reches, Yuval Yaron, Kathryn Burdon, et al.
Human Reproduction (Oxford, England)|May 5, 2017
The ovarian response in fragile X patients and premutation carriers undergoing IVF-PGD: reappraisalSarit Avraham, Benny Almog, Adi Reches, et al.
Fertility and Sterility|June 2, 2009
The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosisGuy Bibi, Mira Malcov, Yaron Yuval, et al.
Journal of Assisted Reproduction and Genetics|February 1, 2023
The association between a carrier state of FMR1 premutation and numeric sex chromosome variationsMira Malcov, Ophir Blickstein, Dana Brabbing-Goldstein, et al.
Prenatal Diagnosis|January 6, 2010
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropeniaMira Malcov, Adi Reches, Dalit Ben-Yosef, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 16, 2018
Whole-exome sequencing in fetuses with central nervous system abnormalitiesAdi Reches, Liran Hiersch, Sharon Simchoni, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
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|March 8, 2018
The genetic and clinical outcome of isolated fetal muscular ventricular septal defect (VSD)Ran Svirsky, Dana Brabbing-Goldstein, Uri Rozovski, et al.
Prenatal Diagnosis|December 20, 2008
Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?Adi Reches, Mira Malcov, Dalit Ben-Yosef, et al.
Plos One|March 16, 2022
NK-92 cells retain vitality and functionality when grown in standard cell culture conditionsRebecca Kotzur, Alexandra Duev-Cohen, Inbal Kol, et al.
Fertility and Sterility|May 11, 2020
Bypassing physiological puberty, a novel procedure of oocyte cryopreservation at age 7: a case report and review of the literatureFoad Azem, Avivit Brener, Gustavo Malinger, et al.
Prenatal Diagnosis|April 25, 2007
Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended familyAdi Reches, Yuval Yaron, Kathryn Burdon, et al.
Human Reproduction (Oxford, England)|May 5, 2017
The ovarian response in fragile X patients and premutation carriers undergoing IVF-PGD: reappraisalSarit Avraham, Benny Almog, Adi Reches, et al.
Fertility and Sterility|June 2, 2009
The effect of CGG repeat number on ovarian response among fragile X premutation carriers undergoing preimplantation genetic diagnosisGuy Bibi, Mira Malcov, Yaron Yuval, et al.
Journal of Assisted Reproduction and Genetics|February 1, 2023
The association between a carrier state of FMR1 premutation and numeric sex chromosome variationsMira Malcov, Ophir Blickstein, Dana Brabbing-Goldstein, et al.
Prenatal Diagnosis|January 6, 2010
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropeniaMira Malcov, Adi Reches, Dalit Ben-Yosef, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 16, 2018
Whole-exome sequencing in fetuses with central nervous system abnormalitiesAdi Reches, Liran Hiersch, Sharon Simchoni, et al.
Pageof 5