Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Sharon Zeligson

Showing results (1-10 of 37) with videos related to

Pageof 4
Sort By:
Journal of Child Neurology|April 25, 2018
Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 DeletionTal Gilboa, Reeval Segel, Sharon Zeligson, et al.
European Journal of Endocrinology|May 24, 2012
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitaliaOded Breuer, Maha Abdulhadi-Atwan, Sharon Zeligson, 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.
Biochemical and Biophysical Research Communications|March 17, 2006
Nanog transforms NIH3T3 cells and targets cell-type restricted genesDan Piestun, Bose S Kochupurakkal, Jasmine Jacob-Hirsch, 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.
Journal of Assisted Reproduction and Genetics|January 14, 2021
Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?Keren Rotshenker-Olshinka, Naama Srebnik Moshe, Omri Weiss, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD)Ziva Ben-Neriah, Rachel Michaelson-Cohen, Michal Inbar-Feigenberg, et al.
Molecular Genetics & Genomic Medicine|July 14, 2018
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi maleTalia Eldar-Geva, Varda Gross-Tsur, Harry J Hirsch, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
Journal of Child Neurology|April 25, 2018
Ganglioglioma, Epilepsy, and Intellectual Impairment due to Familial TSC1 DeletionTal Gilboa, Reeval Segel, Sharon Zeligson, et al.
European Journal of Endocrinology|May 24, 2012
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitaliaOded Breuer, Maha Abdulhadi-Atwan, Sharon Zeligson, 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.
Biochemical and Biophysical Research Communications|March 17, 2006
Nanog transforms NIH3T3 cells and targets cell-type restricted genesDan Piestun, Bose S Kochupurakkal, Jasmine Jacob-Hirsch, 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.
Journal of Assisted Reproduction and Genetics|January 14, 2021
Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?Keren Rotshenker-Olshinka, Naama Srebnik Moshe, Omri Weiss, et al.
American Journal of Human Genetics|January 25, 2011
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndromeRuth Belostotsky, Efrat Ben-Shalom, Choni Rinat, et al.
American Journal of Medical Genetics. Part A|October 13, 2011
A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD)Ziva Ben-Neriah, Rachel Michaelson-Cohen, Michal Inbar-Feigenberg, et al.
Molecular Genetics & Genomic Medicine|July 14, 2018
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi maleTalia Eldar-Geva, Varda Gross-Tsur, Harry J Hirsch, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
Pageof 4