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Yuval Yaron

Showing results (11-20 of 122) with videos related to

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European Journal of Medical Genetics|January 9, 2021
Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotypeDana Brabbing-Goldstein, Yuval Yaron, Adi Reches
Prenatal Diagnosis|March 10, 2026
Variation in the Genetic Workup of Polyhydramnios: An International and Inter-Specialty SurveyRoni Zemet, Yuval Yaron, Lena Sagi-Dain
Obstetrics and Gynecology|October 8, 2015
Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA TechnologyYuval Yaron, Jacques Jani, Maximilian Schmid, et al.
Best Practice & Research. Clinical Obstetrics & Gynaecology|December 12, 2002
ScreeningMark I Evans, Eric L Krivchenia, Yuval Yaron
Prenatal Diagnosis|May 18, 2021
Economic impact of using maternal plasma cell-free DNA testing to guide further workup in recurrent pregnancy lossSiyang Peng, Sucheta Bhatt, Antoni Borrell, et al.
Prenatal Diagnosis|November 18, 2008
Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?Caroline M Ogilvie, Yuval Yaron, Arthur L Beaudet
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|December 8, 2016
Does the number of previous miscarriages influence the incidence of chromosomal aberrations in spontaneous pregnancy loss?Myriam Goldstein, Ran Svirsky, Adi Reches, et al.
Molecular and Cellular Endocrinology|January 8, 2008
Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysisTsvia Frumkin, Mira Malcov, Yuval Yaron, et al.
Fetal Diagnosis and Therapy|June 8, 2006
Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reactionYifat Ochshorn, Anat Bar-Shira, Anat Jonish, et al.
Prenatal Diagnosis|July 2, 2004
First-trimester nuchal translucency and maternal serum free beta-hCG and PAPP-A can detect triploidy and determine the parental originYuval Yaron, Yifat Ochshorn, Sigal Tsabari, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
European Journal of Medical Genetics|January 9, 2021
Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotypeDana Brabbing-Goldstein, Yuval Yaron, Adi Reches
Prenatal Diagnosis|March 10, 2026
Variation in the Genetic Workup of Polyhydramnios: An International and Inter-Specialty SurveyRoni Zemet, Yuval Yaron, Lena Sagi-Dain
Obstetrics and Gynecology|October 8, 2015
Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA TechnologyYuval Yaron, Jacques Jani, Maximilian Schmid, et al.
Best Practice & Research. Clinical Obstetrics & Gynaecology|December 12, 2002
ScreeningMark I Evans, Eric L Krivchenia, Yuval Yaron
Prenatal Diagnosis|May 18, 2021
Economic impact of using maternal plasma cell-free DNA testing to guide further workup in recurrent pregnancy lossSiyang Peng, Sucheta Bhatt, Antoni Borrell, et al.
Prenatal Diagnosis|November 18, 2008
Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?Caroline M Ogilvie, Yuval Yaron, Arthur L Beaudet
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|December 8, 2016
Does the number of previous miscarriages influence the incidence of chromosomal aberrations in spontaneous pregnancy loss?Myriam Goldstein, Ran Svirsky, Adi Reches, et al.
Molecular and Cellular Endocrinology|January 8, 2008
Elucidating the origin of chromosomal aberrations in IVF embryos by preimplantation genetic analysisTsvia Frumkin, Mira Malcov, Yuval Yaron, et al.
Fetal Diagnosis and Therapy|June 8, 2006
Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reactionYifat Ochshorn, Anat Bar-Shira, Anat Jonish, et al.
Prenatal Diagnosis|July 2, 2004
First-trimester nuchal translucency and maternal serum free beta-hCG and PAPP-A can detect triploidy and determine the parental originYuval Yaron, Yifat Ochshorn, Sigal Tsabari, et al.
Pageof 13