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 (91-100 of 11,257) with videos related to

Pageof 1,126
Sort By:
Human Genetics|May 19, 1976
Tricho-rhino-phalangeal syndrome. The first case in JapanN Fukushima, M Anakura, S Arashima, et al.
Human Genetics|May 19, 1976
Pathomorphological changes in an early spontaneous abortus with triploidy (69, XXX)V P Kulazenko, L G Kulazenko
Human Genetics|April 24, 2003
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosisSandrine Haut, Michèle Brivet, Guy Touati, et al.
Human Genetics|April 15, 1976
Origin of the extra chromosome no. 21 in Down's syndromeP Wagenbichler, W Killian, A Rett, et al.
Human Genetics|July 29, 2003
Relationship between serum HDL-C levels and common genetic variants of the endothelial lipase gene in Japanese school-aged childrenKimiko Yamakawa-Kobayashi, Hisako Yanagi, Kazue Endo, et al.
Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y Suzuki
Human Genetics|May 22, 2003
The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and DongxiangWei Wang, Cheryl Wise, Tom Baric, et al.
Human Genetics|March 18, 2003
Fetal DNA in maternal serum: does it persist after pregnancy?Alexandra Benachi, Julie Steffann, Evelyne Gautier, et al.
Human Genetics|February 22, 2003
Influence of interleukin-12 receptor beta1 polymorphisms on tuberculosisMitsuteru Akahoshi, Hitoshi Nakashima, Katsuhisa Miyake, et al.
Human Genetics|February 22, 2003
FMR1 haplotype analyses among Indians: a weak founder effect and other findingsDeepti Sharma, Meena Gupta, B K Thelma
Pageof 1,126

Showing results (91-100 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|May 19, 1976
Tricho-rhino-phalangeal syndrome. The first case in JapanN Fukushima, M Anakura, S Arashima, et al.
Human Genetics|May 19, 1976
Pathomorphological changes in an early spontaneous abortus with triploidy (69, XXX)V P Kulazenko, L G Kulazenko
Human Genetics|April 24, 2003
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosisSandrine Haut, Michèle Brivet, Guy Touati, et al.
Human Genetics|April 15, 1976
Origin of the extra chromosome no. 21 in Down's syndromeP Wagenbichler, W Killian, A Rett, et al.
Human Genetics|July 29, 2003
Relationship between serum HDL-C levels and common genetic variants of the endothelial lipase gene in Japanese school-aged childrenKimiko Yamakawa-Kobayashi, Hisako Yanagi, Kazue Endo, et al.
Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y Suzuki
Human Genetics|May 22, 2003
The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and DongxiangWei Wang, Cheryl Wise, Tom Baric, et al.
Human Genetics|March 18, 2003
Fetal DNA in maternal serum: does it persist after pregnancy?Alexandra Benachi, Julie Steffann, Evelyne Gautier, et al.
Human Genetics|February 22, 2003
Influence of interleukin-12 receptor beta1 polymorphisms on tuberculosisMitsuteru Akahoshi, Hitoshi Nakashima, Katsuhisa Miyake, et al.
Human Genetics|February 22, 2003
FMR1 haplotype analyses among Indians: a weak founder effect and other findingsDeepti Sharma, Meena Gupta, B K Thelma
Pageof 1,126