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

Dorit Lev

Showing results (131-140 of 176) with videos related to

Pageof 18
Sort By:
Human Mutation|September 25, 2022
Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33AElena V Pavlova, Dorit Lev, Marina Michelson, 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|November 23, 2020
Procedure-to-delivery interval after late amniocentesis and the need for routine antenatal corticosteroidsSophia Leytes, Karina Krajden Haratz, Leonti Grin, et al.
American Journal of Human Genetics|October 6, 2010
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophyOrly Agamy, Bruria Ben Zeev, Dorit Lev, et al.
Molecular Genetics and Metabolism|December 7, 2007
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish originIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Journal of Neurology|September 10, 2014
Costeff syndrome: clinical features and natural historyGilad Yahalom, Yair Anikster, Ruth Huna-Baron, et al.
International Journal of Biometeorology|July 1, 2005
Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990-2000Eliahu G Stoupel, Helena Frimer, Zvi Appelman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 14, 2018
The cerebellar "tilted telephone receiver sign" enables prenatal diagnosis of PHACES syndromeZvi Leibovitz, Laurent Guibaud, Catherine Garel, et al.
Journal of the National Cancer Institute|May 8, 2003
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndromeLisa L Wang, Anu Gannavarapu, Claudia A Kozinetz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2020
Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological featuresLubov Blumkin, Zvi Leibovitz, Karina Krajden-Haratz, et al.
Annals of Neurology|March 14, 2018
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathyMitsuko Nakashima, Mitsuhiro Kato, Kazushi Aoto, et al.
Pageof 18

Showing results (131-140 of 176) with videos related to

Sort By:
Pageof 18
Human Mutation|September 25, 2022
Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33AElena V Pavlova, Dorit Lev, Marina Michelson, 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|November 23, 2020
Procedure-to-delivery interval after late amniocentesis and the need for routine antenatal corticosteroidsSophia Leytes, Karina Krajden Haratz, Leonti Grin, et al.
American Journal of Human Genetics|October 6, 2010
Mutations disrupting selenocysteine formation cause progressive cerebello-cerebral atrophyOrly Agamy, Bruria Ben Zeev, Dorit Lev, et al.
Molecular Genetics and Metabolism|December 7, 2007
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish originIngrid Tein, Orly Elpeleg, Bruria Ben-Zeev, et al.
Journal of Neurology|September 10, 2014
Costeff syndrome: clinical features and natural historyGilad Yahalom, Yair Anikster, Ruth Huna-Baron, et al.
International Journal of Biometeorology|July 1, 2005
Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990-2000Eliahu G Stoupel, Helena Frimer, Zvi Appelman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 14, 2018
The cerebellar "tilted telephone receiver sign" enables prenatal diagnosis of PHACES syndromeZvi Leibovitz, Laurent Guibaud, Catherine Garel, et al.
Journal of the National Cancer Institute|May 8, 2003
Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndromeLisa L Wang, Anu Gannavarapu, Claudia A Kozinetz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 15, 2020
Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological featuresLubov Blumkin, Zvi Leibovitz, Karina Krajden-Haratz, et al.
Annals of Neurology|March 14, 2018
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathyMitsuko Nakashima, Mitsuhiro Kato, Kazushi Aoto, et al.
Pageof 18