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

Human genetics

Showing results (691-700 of 11,264) with videos related to

Pageof 1,127
Sort By:
Human Genetics|June 1, 1988
Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemiaT Funahashi, Y Miyake, A Yamamoto, et al.
Human Genetics|June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14D A Robertson, D F Callen, E G Baker, et al.
Human Genetics|August 18, 2021
Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variantChris Rorden, Marilee C Griswold, Nan Moses, et al.
Human Genetics|August 21, 2021
ASL expression in ALDH1A1<sup>+</sup> neurons in the substantia nigra metabolically contributes to neurodegenerative phenotypeShaul Lerner, Raya Eilam, Lital Adler, et al.
Human Genetics|July 25, 2015
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genesNicola H Chapman, Alejandro Q Nato, Raphael Bernier, et al.
Human Genetics|April 15, 2020
Human genetic basis of fulminant viral hepatitisEmmanuelle Jouanguy
Human Genetics|May 10, 1977
Origin of the translocated segment of the 14q+ marker in non-Burkitt lymphomasJ Mark, C Ekedahl, A Hagman
Human Genetics|August 19, 2016
Biomedical applications of gene editingPablo Perez-Pinera, Zheng-Yi Chen
Human Genetics|January 1, 1982
The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolutionF Pasquali, C Panarello, P Bernasconi, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Pageof 1,127

Showing results (691-700 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|June 1, 1988
Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemiaT Funahashi, Y Miyake, A Yamamoto, et al.
Human Genetics|June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14D A Robertson, D F Callen, E G Baker, et al.
Human Genetics|August 18, 2021
Radiographical Survey of Osteochondrodysplasia in Scottish Fold Cats caused by the TRPV4 gene variantChris Rorden, Marilee C Griswold, Nan Moses, et al.
Human Genetics|August 21, 2021
ASL expression in ALDH1A1<sup>+</sup> neurons in the substantia nigra metabolically contributes to neurodegenerative phenotypeShaul Lerner, Raya Eilam, Lital Adler, et al.
Human Genetics|July 25, 2015
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genesNicola H Chapman, Alejandro Q Nato, Raphael Bernier, et al.
Human Genetics|April 15, 2020
Human genetic basis of fulminant viral hepatitisEmmanuelle Jouanguy
Human Genetics|May 10, 1977
Origin of the translocated segment of the 14q+ marker in non-Burkitt lymphomasJ Mark, C Ekedahl, A Hagman
Human Genetics|August 19, 2016
Biomedical applications of gene editingPablo Perez-Pinera, Zheng-Yi Chen
Human Genetics|January 1, 1982
The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolutionF Pasquali, C Panarello, P Bernasconi, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Pageof 1,127