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Shay Ben-Shachar

Showing results (31-40 of 96) with videos related to

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American Journal of Medical Genetics. Part A|April 20, 2017
Cranial irradiation in childhood mimicking neurofibromatosis type IIFelix Bokstein, Tom Dubov, Hagit Toledano-Alhadef, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
Obstetrics and Gynecology|December 5, 2020
Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mmLena Sagi-Dain, Amihood Singer, Shay Ben Shachar, et al.
Journal of Clinical Immunology|May 29, 2021
MHC Haplotyping of SARS-CoV-2 Patients: HLA Subtypes Are Not Associated with the Presence and Severity of COVID-19 in the Israeli PopulationShay Ben Shachar, Noam Barda, Sigal Manor, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 8, 2018
Prenatal microarray analysis in right aortic arch-a retrospective cohort study and review of the literatureIdit Maya, Amihood Singer, Hagit N Baris, et al.
Journal of Molecular Neuroscience : MN|September 16, 2017
Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted PopulationShay Ben-Shachar, Zaid Afawi, Rafik Masalha, et al.
Journal of the American Academy of Dermatology|March 21, 2017
Predicting neurofibromatosis type 1 risk among children with isolated café-au-lait maculesShay Ben-Shachar, Tom Dubov, Hagit Toledano-Alhadef, et al.
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|April 30, 2019
Is fetal isolated double renal collecting system an indication for chromosomal microarray?Amihood Singer, Idit Maya, Ayala Frumkin, et al.
Prenatal Diagnosis|March 11, 2014
Microscopic chromosome Xp distal deletions--a challenging issue in prenatal genetic counselingRivka Sukenik-Halevy, Adi Reches, Anat Bar-Shira, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|April 20, 2017
Cranial irradiation in childhood mimicking neurofibromatosis type IIFelix Bokstein, Tom Dubov, Hagit Toledano-Alhadef, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 31, 2014
Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi womenKarin Weiss, Avi Orr-Urtreger, Idit Kaplan Ber, et al.
Obstetrics and Gynecology|December 5, 2020
Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mmLena Sagi-Dain, Amihood Singer, Shay Ben Shachar, et al.
Journal of Clinical Immunology|May 29, 2021
MHC Haplotyping of SARS-CoV-2 Patients: HLA Subtypes Are Not Associated with the Presence and Severity of COVID-19 in the Israeli PopulationShay Ben Shachar, Noam Barda, Sigal Manor, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|February 8, 2018
Prenatal microarray analysis in right aortic arch-a retrospective cohort study and review of the literatureIdit Maya, Amihood Singer, Hagit N Baris, et al.
Journal of Molecular Neuroscience : MN|September 16, 2017
Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted PopulationShay Ben-Shachar, Zaid Afawi, Rafik Masalha, et al.
Journal of the American Academy of Dermatology|March 21, 2017
Predicting neurofibromatosis type 1 risk among children with isolated café-au-lait maculesShay Ben-Shachar, Tom Dubov, Hagit Toledano-Alhadef, et al.
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|April 30, 2019
Is fetal isolated double renal collecting system an indication for chromosomal microarray?Amihood Singer, Idit Maya, Ayala Frumkin, et al.
Prenatal Diagnosis|March 11, 2014
Microscopic chromosome Xp distal deletions--a challenging issue in prenatal genetic counselingRivka Sukenik-Halevy, Adi Reches, Anat Bar-Shira, et al.
Pageof 10