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

Doron M Behar

Showing results (11-20 of 90) with videos related to

Pageof 9
Sort By:
Human Heredity|September 15, 2017
Consanguinity Rates Predict Long Runs of Homozygosity in Jewish PopulationsJonathan T L Kang, Amy Goldberg, Michael D Edge, et al.
Molecular Genetics and Metabolism|February 6, 2007
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patientLiat Benayoun, Esther Granot, Leah Rizel, et al.
Genetic Testing and Molecular Biomarkers|December 26, 2013
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestryDoron M Behar, Bella Davidov, Zippora Brownstein, et al.
Scientific Reports|December 13, 2019
West Asian sources of the Eurasian component in Ethiopians: a reassessmentLudovica Molinaro, Francesco Montinaro, Burak Yelmen, et al.
The Journal of Clinical Endocrinology and Metabolism|July 26, 2014
Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiencyLiat de Vries, Doron M Behar, Pola Smirin-Yosef, et al.
Genetics|September 16, 2008
Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classificationSaharon Rosset, R Spencer Wells, David F Soria-Hernanz, et al.
Journal of Clinical Microbiology|October 2, 2002
Molecular epidemiological analysis of the changing nature of a meningococcal outbreak following a vaccination campaignLiran I Shlush, Doron M Behar, Adrian Zelazny, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Plos One|May 8, 2008
The Druze: a population genetic refugium of the Near EastLiran I Shlush, Doron M Behar, Guennady Yudkovsky, et al.
BMC Evolutionary Biology|December 5, 2012
Divorcing the Late Upper Palaeolithic demographic histories of mtDNA haplogroups M1 and U6 in AfricaErwan Pennarun, Toomas Kivisild, Ene Metspalu, et al.
Pageof 9

Showing results (11-20 of 90) with videos related to

Sort By:
Pageof 9
Human Heredity|September 15, 2017
Consanguinity Rates Predict Long Runs of Homozygosity in Jewish PopulationsJonathan T L Kang, Amy Goldberg, Michael D Edge, et al.
Molecular Genetics and Metabolism|February 6, 2007
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patientLiat Benayoun, Esther Granot, Leah Rizel, et al.
Genetic Testing and Molecular Biomarkers|December 26, 2013
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestryDoron M Behar, Bella Davidov, Zippora Brownstein, et al.
Scientific Reports|December 13, 2019
West Asian sources of the Eurasian component in Ethiopians: a reassessmentLudovica Molinaro, Francesco Montinaro, Burak Yelmen, et al.
The Journal of Clinical Endocrinology and Metabolism|July 26, 2014
Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiencyLiat de Vries, Doron M Behar, Pola Smirin-Yosef, et al.
Genetics|September 16, 2008
Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classificationSaharon Rosset, R Spencer Wells, David F Soria-Hernanz, et al.
Journal of Clinical Microbiology|October 2, 2002
Molecular epidemiological analysis of the changing nature of a meningococcal outbreak following a vaccination campaignLiran I Shlush, Doron M Behar, Adrian Zelazny, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 19, 2014
Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22Rony Cohen, Lina Basel-Vanagaite, Hadassah Goldberg-Stern, et al.
Plos One|May 8, 2008
The Druze: a population genetic refugium of the Near EastLiran I Shlush, Doron M Behar, Guennady Yudkovsky, et al.
BMC Evolutionary Biology|December 5, 2012
Divorcing the Late Upper Palaeolithic demographic histories of mtDNA haplogroups M1 and U6 in AfricaErwan Pennarun, Toomas Kivisild, Ene Metspalu, et al.
Pageof 9