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

M Behar

Showing results (301-310 of 373) with videos related to

Pageof 38
Sort By:
European Journal of Human Genetics : EJHG|September 8, 2016
Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin CEyal Reinstein, Ana Gutierrez-Fernandez, Shay Tzur, et al.
Human Molecular Genetics|August 4, 2006
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency allelesPaul Verdu, Luis B Barreiro, Etienne Patin, et al.
American Journal of Human Genetics|January 18, 2006
Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genesEtienne Patin, Luis B Barreiro, Pardis C Sabeti, et al.
American Journal of Human Genetics|April 29, 2008
The dawn of human matrilineal diversityDoron M Behar, Richard Villems, Himla Soodyall, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
Pacing and Clinical Electrophysiology : PACE|January 19, 2022
The long-term outcomes of cardiac implantable electronic devices implanted via the femoral routeSamuel Griffiths, Jonathan M Behar, Daniel B Kramer, et al.
Human Mutation|February 4, 2015
Mutations in TAX1BP3 cause dilated cardiomyopathy with septo-optic dysplasiaEyal Reinstein, Katia Orvin, Einav Tayeb-Fligelman, et al.
Journal of Internal Medicine|November 22, 2025
T cell-macrophage interactions in tuberculosis: What we've got here is failure to communicateRasmus Mortensen, Cecilia S Lindestam Arlehamn, Rhea N Coler, et al.
BMC Genetics|September 2, 2004
Most of the extant mtDNA boundaries in south and southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humansMait Metspalu, Toomas Kivisild, Ene Metspalu, et al.
Familial Cancer|June 14, 2017
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in IsraelNaim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, et al.
Pageof 38

Showing results (301-310 of 373) with videos related to

Sort By:
Pageof 38
European Journal of Human Genetics : EJHG|September 8, 2016
Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin CEyal Reinstein, Ana Gutierrez-Fernandez, Shay Tzur, et al.
Human Molecular Genetics|August 4, 2006
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency allelesPaul Verdu, Luis B Barreiro, Etienne Patin, et al.
American Journal of Human Genetics|January 18, 2006
Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genesEtienne Patin, Luis B Barreiro, Pardis C Sabeti, et al.
American Journal of Human Genetics|April 29, 2008
The dawn of human matrilineal diversityDoron M Behar, Richard Villems, Himla Soodyall, et al.
Endocrine|May 7, 2020
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSDFloris Levy-Khademi, Sharon Zeligson, Eran Lavi, et al.
Pacing and Clinical Electrophysiology : PACE|January 19, 2022
The long-term outcomes of cardiac implantable electronic devices implanted via the femoral routeSamuel Griffiths, Jonathan M Behar, Daniel B Kramer, et al.
Human Mutation|February 4, 2015
Mutations in TAX1BP3 cause dilated cardiomyopathy with septo-optic dysplasiaEyal Reinstein, Katia Orvin, Einav Tayeb-Fligelman, et al.
Journal of Internal Medicine|November 22, 2025
T cell-macrophage interactions in tuberculosis: What we've got here is failure to communicateRasmus Mortensen, Cecilia S Lindestam Arlehamn, Rhea N Coler, et al.
BMC Genetics|September 2, 2004
Most of the extant mtDNA boundaries in south and southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humansMait Metspalu, Toomas Kivisild, Ene Metspalu, et al.
Familial Cancer|June 14, 2017
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in IsraelNaim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, et al.
Pageof 38