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Shay Ben-Shachar

Showing results (21-30 of 96) with videos related to

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American Journal of Medical Genetics. Part A|January 28, 2017
Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis ComplexJonah Fox, Shay Ben-Shachar, Shimrit Uliel, et al.
European Journal of Public Health|April 1, 2026
Psychologically informed reminder messages for promoting BRCA1/2 carrier screening: evidence from a large-scale population-based studyTom Mushkat, Rotem Greenberg, Ofer Isakov, et al.
Journal of Perinatal Medicine|December 8, 2019
Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature reviewAmihood Singer, Idit Maya, Rivka Sukenik-Halevy, et al.
Early Human Development|April 28, 2020
Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnanciesAmihood Singer, Idit Maya, Ehud Banne, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2025
No association between FMR1 premutation and either ADHD or anxiety in 53,707 women undergoing genetic testing for family planning purposesLiraz Klausner, Shai Carmi, Shay Ben-Shachar, et al.
Journal of Pediatric Genetics|April 29, 2020
Clinical Observation: Effect of a Second Transpositioned Variant in a Family with Autosomal Dominant Ryanodine Receptor-1-Related DiseaseTomer Avnon, Ran Svirsky, Avi Orr-Urtreger, et al.
Inflammatory Bowel Diseases|September 29, 2018
Genotype-Serotype Interactions Shed Light on Genetic Components of Inflammatory Bowel DiseasesShay Ben-Shachar, Yael Finezilber, Hofit Elad, et al.
Inflammatory Bowel Diseases|April 25, 2018
Increase in Processing Factors Is Involved in Skewed MicroRNA Expression in Patients with Ulcerative Colitis Who Develop Small Intestine Inflammation after Pouch SurgeryHadas Sherman Horev, Keren M Rabinowitz, Hofit Elad, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 20, 2019
What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?Idit Maya, Amihood Singer, Hagith Yonath, et al.
European Journal of Human Genetics : EJHG|October 11, 2012
Increased rate of missense/in-frame mutations in individuals with NF1-related pulmonary stenosis: a novel genotype-phenotype correlationShay Ben-Shachar, Shlomi Constantini, Hen Hallevi, et al.
Pageof 10

Showing results (21-30 of 96) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|January 28, 2017
Rare familial TSC2 gene mutation associated with atypical phenotype presentation of Tuberous Sclerosis ComplexJonah Fox, Shay Ben-Shachar, Shimrit Uliel, et al.
European Journal of Public Health|April 1, 2026
Psychologically informed reminder messages for promoting BRCA1/2 carrier screening: evidence from a large-scale population-based studyTom Mushkat, Rotem Greenberg, Ofer Isakov, et al.
Journal of Perinatal Medicine|December 8, 2019
Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature reviewAmihood Singer, Idit Maya, Rivka Sukenik-Halevy, et al.
Early Human Development|April 28, 2020
Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnanciesAmihood Singer, Idit Maya, Ehud Banne, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2025
No association between FMR1 premutation and either ADHD or anxiety in 53,707 women undergoing genetic testing for family planning purposesLiraz Klausner, Shai Carmi, Shay Ben-Shachar, et al.
Journal of Pediatric Genetics|April 29, 2020
Clinical Observation: Effect of a Second Transpositioned Variant in a Family with Autosomal Dominant Ryanodine Receptor-1-Related DiseaseTomer Avnon, Ran Svirsky, Avi Orr-Urtreger, et al.
Inflammatory Bowel Diseases|September 29, 2018
Genotype-Serotype Interactions Shed Light on Genetic Components of Inflammatory Bowel DiseasesShay Ben-Shachar, Yael Finezilber, Hofit Elad, et al.
Inflammatory Bowel Diseases|April 25, 2018
Increase in Processing Factors Is Involved in Skewed MicroRNA Expression in Patients with Ulcerative Colitis Who Develop Small Intestine Inflammation after Pouch SurgeryHadas Sherman Horev, Keren M Rabinowitz, Hofit Elad, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 20, 2019
What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?Idit Maya, Amihood Singer, Hagith Yonath, et al.
European Journal of Human Genetics : EJHG|October 11, 2012
Increased rate of missense/in-frame mutations in individuals with NF1-related pulmonary stenosis: a novel genotype-phenotype correlationShay Ben-Shachar, Shlomi Constantini, Hen Hallevi, et al.
Pageof 10