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 (391-400 of 11,264) with videos related to

Pageof 1,127
Sort By:
Human Genetics|July 26, 1977
The 48, XXXX/49,XXXXY/49,XXXX,i(Yq) mosaicism in a 3-year-old boy from a twin pregnancyB Kaluzewski, D Podkul, I Zaborowska, et al.
Human Genetics|September 1, 1995
A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysisA M Barbieri, N Soriani, G M Tubiello, et al.
Human Genetics|September 1, 1995
Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variantJ A Luyten, P W Wenink, G C Steenbergen-Spanjers, et al.
Human Genetics|July 1, 1995
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 geneE K Bijlsma, P Merel, P Fleury, et al.
Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M Anvret
Human Genetics|July 1, 1995
Detection and characterization of new mutations in the human angiotensinogen gene (AGT)J E Hixson, P K Powers
Human Genetics|July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literatureC M Tuck-Muller, H Chen, J E Martínez, et al.
Human Genetics|July 1, 1995
Detection of a CfoI polymorphism within exon 5 of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene (CHRNA4)O Steinlein
Human Genetics|July 1, 1995
Transferable clastogenic activity in plasma from patients with Fanconi anemiaI Emerit, A Levy, G Pagano, et al.
Human Genetics|July 1, 1995
Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemiaC Sass, L M Giroux, Y Ma, et al.
Pageof 1,127

Showing results (391-400 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|July 26, 1977
The 48, XXXX/49,XXXXY/49,XXXX,i(Yq) mosaicism in a 3-year-old boy from a twin pregnancyB Kaluzewski, D Podkul, I Zaborowska, et al.
Human Genetics|September 1, 1995
A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysisA M Barbieri, N Soriani, G M Tubiello, et al.
Human Genetics|September 1, 1995
Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variantJ A Luyten, P W Wenink, G C Steenbergen-Spanjers, et al.
Human Genetics|July 1, 1995
Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 geneE K Bijlsma, P Merel, P Fleury, et al.
Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M Anvret
Human Genetics|July 1, 1995
Detection and characterization of new mutations in the human angiotensinogen gene (AGT)J E Hixson, P K Powers
Human Genetics|July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literatureC M Tuck-Muller, H Chen, J E Martínez, et al.
Human Genetics|July 1, 1995
Detection of a CfoI polymorphism within exon 5 of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene (CHRNA4)O Steinlein
Human Genetics|July 1, 1995
Transferable clastogenic activity in plasma from patients with Fanconi anemiaI Emerit, A Levy, G Pagano, et al.
Human Genetics|July 1, 1995
Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemiaC Sass, L M Giroux, Y Ma, et al.
Pageof 1,127