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Yuval Yaron

Showing results (61-70 of 122) with videos related to

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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.
Human Reproduction (Oxford, England)|February 1, 2002
Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilizationYuval Yaron, Ofer Lehavi, Avi Orr-Urtreger, 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.
Prenatal Diagnosis|January 8, 2025
A Missense Variant in KIF14 Results in Two Gene Isoforms by Affecting Normal Gene SplicingDorin Trigubov, Vered Ofen-Glassner, Bar Levy, et al.
Human Mutation|May 15, 2002
Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutationsNancy Gavert, Yuval Yaron, Tova Naiman, et al.
Reproductive Biomedicine Online|April 12, 2007
Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCRMira Malcov, Tova Naiman, Dalit Ben Yosef, et al.
Prenatal Diagnosis|August 28, 2023
SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetranceNoa Hourvitz, Alina Kurolap, Adi Mory, et al.
Prenatal Diagnosis|March 21, 2017
Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methodsCarlo G Artieri, Carrie Haverty, Eric A Evans, et al.
Fertility and Sterility|October 3, 2008
Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potentialShiri Barbash-Hazan, Tsvia Frumkin, Mira Malcov, et al.
Molecular Genetics and Metabolism|September 6, 2012
A founder mutation causing a severe methylenetetrahydrofolate reductase (MTHFR) deficiency in Bukharian JewsShay Ben-Shachar, Tal Zvi, Arndt Rolfs, et al.
Pageof 13

Showing results (61-70 of 122) with videos related to

Sort By:
Pageof 13
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.
Human Reproduction (Oxford, England)|February 1, 2002
Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilizationYuval Yaron, Ofer Lehavi, Avi Orr-Urtreger, 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.
Prenatal Diagnosis|January 8, 2025
A Missense Variant in KIF14 Results in Two Gene Isoforms by Affecting Normal Gene SplicingDorin Trigubov, Vered Ofen-Glassner, Bar Levy, et al.
Human Mutation|May 15, 2002
Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutationsNancy Gavert, Yuval Yaron, Tova Naiman, et al.
Reproductive Biomedicine Online|April 12, 2007
Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCRMira Malcov, Tova Naiman, Dalit Ben Yosef, et al.
Prenatal Diagnosis|August 28, 2023
SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetranceNoa Hourvitz, Alina Kurolap, Adi Mory, et al.
Prenatal Diagnosis|March 21, 2017
Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methodsCarlo G Artieri, Carrie Haverty, Eric A Evans, et al.
Fertility and Sterility|October 3, 2008
Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potentialShiri Barbash-Hazan, Tsvia Frumkin, Mira Malcov, et al.
Molecular Genetics and Metabolism|September 6, 2012
A founder mutation causing a severe methylenetetrahydrofolate reductase (MTHFR) deficiency in Bukharian JewsShay Ben-Shachar, Tal Zvi, Arndt Rolfs, et al.
Pageof 13