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

V Meiner

Showing results (11-20 of 42) with videos related to

Pageof 5
Sort By:
Journal of Neurology|July 1, 1997
Intrafamilial heterogeneity of movement disorders: report of three cases in one familyA Lossos, O Cohen, V Meiner, et al.
Human Molecular Genetics|January 1, 1994
Premature termination codon at the sterol 27-hydroxylase gene causes cerebrotendinous xanthomatosis in an Afrikaner familyV Meiner, D A Marais, A Reshef, et al.
Public Health Genomics|July 3, 2013
Clinicians' attitudes toward general screening of the Ashkenazi-Jewish population for prevalent founder BRCA1/2 and LRRK2 mutationsS Shkedi-Rafid, G Ofer-Bialer, V Meiner, et al.
Human Genetics|May 1, 1992
Prenatal diagnosis of familial hypercholesterolemia caused by the "Lebanese" mutation at the low density lipoprotein receptor locusA Reshef, V Meiner, E J Dann, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomesD Abeliovich, J Dagan, M Werner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau geneD J Gross, N Avishai, V Meiner, et al.
Clinical Genetics|July 28, 2018
Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasiaE B Cadoff, R Sheffer, S Wientroub, et al.
Journal of Intellectual Disability Research : JIDR|March 30, 2007
Deletions of VCX-A and NLGN4: a variable phenotype including normal intellectM Macarov, M Zeigler, J P Newman, et al.
Journal of Forensic Sciences|September 16, 1999
Chorionic villus sampling prior to pregnancy termination, a tool for forensic paternity testingA Reshef, P Brauner, M Shpitzen, et al.
American Journal of Medical Genetics|July 12, 1996
Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2S Bar-David, I Lerer, C K Sarfaty, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Journal of Neurology|July 1, 1997
Intrafamilial heterogeneity of movement disorders: report of three cases in one familyA Lossos, O Cohen, V Meiner, et al.
Human Molecular Genetics|January 1, 1994
Premature termination codon at the sterol 27-hydroxylase gene causes cerebrotendinous xanthomatosis in an Afrikaner familyV Meiner, D A Marais, A Reshef, et al.
Public Health Genomics|July 3, 2013
Clinicians' attitudes toward general screening of the Ashkenazi-Jewish population for prevalent founder BRCA1/2 and LRRK2 mutationsS Shkedi-Rafid, G Ofer-Bialer, V Meiner, et al.
Human Genetics|May 1, 1992
Prenatal diagnosis of familial hypercholesterolemia caused by the "Lebanese" mutation at the low density lipoprotein receptor locusA Reshef, V Meiner, E J Dann, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomesD Abeliovich, J Dagan, M Werner, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1996
Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau geneD J Gross, N Avishai, V Meiner, et al.
Clinical Genetics|July 28, 2018
Mechanistic insights into the cellular effects of a novel FN1 variant associated with a spondylometaphyseal dysplasiaE B Cadoff, R Sheffer, S Wientroub, et al.
Journal of Intellectual Disability Research : JIDR|March 30, 2007
Deletions of VCX-A and NLGN4: a variable phenotype including normal intellectM Macarov, M Zeigler, J P Newman, et al.
Journal of Forensic Sciences|September 16, 1999
Chorionic villus sampling prior to pregnancy termination, a tool for forensic paternity testingA Reshef, P Brauner, M Shpitzen, et al.
American Journal of Medical Genetics|July 12, 1996
Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2S Bar-David, I Lerer, C K Sarfaty, et al.
Pageof 5