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 (931-940 of 9,569) with videos related to

Pageof 957
Sort By:
Human Genetics|April 1, 1996
SSCP analysis of the tyrosine kinase domain of the insulin receptor gene: polymorphisms detected in South African black and white subjectsV R Panz, P Ruff, B I Joffe, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Human Genetics|April 1, 1996
Acid alpha-glucosidase deficiency: identification and expression of a missense mutation (S529V) in a Japanese adult phenotypeH Tsunoda, T Ohshima, J Tohyama, et al.
Human Genetics|April 1, 1996
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersR J Oostra, S Kemp, P A Bolhuis, et al.
Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.
Human Genetics|April 1, 1996
Congenital alacrima in a patient with G (Opitz Frias) syndromeM Dundar, K Erkihç, F Demiryilmaz, et al.
Human Genetics|March 1, 1996
Fanconi anaemia complementation groups in Germany and The Netherlands. European Fanconi Anaemia Research groupH Joenje
Human Genetics|March 1, 1996
Deletion of a Gly-Pro-Pro repeat in the pro alpha2(I) chain of procollagen I in a family with dominant osteogenesis imperfecta type IVA M Lund, F Skovby, M Schwartz
Human Genetics|March 1, 1996
Inheritance of the S113L mutation within an inbred family with carnitine palmitoyltransferase enzyme deficiencyI Handig, E Dams, F Taroni, et al.
Pageof 957

Showing results (931-940 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|April 1, 1996
SSCP analysis of the tyrosine kinase domain of the insulin receptor gene: polymorphisms detected in South African black and white subjectsV R Panz, P Ruff, B I Joffe, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Human Genetics|April 1, 1996
Acid alpha-glucosidase deficiency: identification and expression of a missense mutation (S529V) in a Japanese adult phenotypeH Tsunoda, T Ohshima, J Tohyama, et al.
Human Genetics|April 1, 1996
No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriersR J Oostra, S Kemp, P A Bolhuis, et al.
Human Genetics|April 1, 1996
Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndromeE Mornet, C Chateau, A Taillandier, et al.
Human Genetics|April 1, 1996
Ablepharon macrostomia syndrome with associated cutis laxa: possible localization to 18qJ E Pellegrino, R E Schnur, L Boghosian-Sell, et al.
Human Genetics|April 1, 1996
Congenital alacrima in a patient with G (Opitz Frias) syndromeM Dundar, K Erkihç, F Demiryilmaz, et al.
Human Genetics|March 1, 1996
Fanconi anaemia complementation groups in Germany and The Netherlands. European Fanconi Anaemia Research groupH Joenje
Human Genetics|March 1, 1996
Deletion of a Gly-Pro-Pro repeat in the pro alpha2(I) chain of procollagen I in a family with dominant osteogenesis imperfecta type IVA M Lund, F Skovby, M Schwartz
Human Genetics|March 1, 1996
Inheritance of the S113L mutation within an inbred family with carnitine palmitoyltransferase enzyme deficiencyI Handig, E Dams, F Taroni, et al.
Pageof 957