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 (771-780 of 9,569) with videos related to

Pageof 957
Sort By:
Human Genetics|April 4, 2000
SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markersI Biunno, L Bernard, P Dear, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Human Genetics|August 30, 1976
Evidence that chromosome band 22q12 is concerned with cell proliferation in chronic myeloid leukaemiaP H Fitzgerald
Human Genetics|August 24, 1999
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathiesR Allikmets, J M Seddon, P S Bernstein, et al.
Human Genetics|August 24, 1999
Gene expression patterns in cell lines from patients with 18q- syndromeZ Wang, J D Cody, R J Leach, et al.
Human Genetics|August 24, 1999
Ancestral origin of variation in the triosephosphate isomerase gene promoterA Humphries, A Ationu, M R Lalloz, et al.
Human Genetics|August 24, 1999
Comparison of complementary and genomic DNA sequencing for the detection of mutations in the HMBS gene in British patients with acute intermittent porphyria: identification of 25 novel mutationsS D Whatley, J R Woolf, G H Elder
Human Genetics|August 24, 1999
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase geneD Pirulli, D Puzzer, L Ferri, et al.
Human Genetics|June 1, 2000
Association of butyrylcholinesterase K variant with cholinesterase-positive neuritic plaques in the temporal cortex in late-onset Alzheimer's diseaseD J Lehmann, Z Nagy, S Litchfield, et al.
Human Genetics|September 15, 2000
Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachyteneE Y Cheng, Y J Chen, C M Disteche, et al.
Pageof 957

Showing results (771-780 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|April 4, 2000
SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markersI Biunno, L Bernard, P Dear, et al.
Human Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.
Human Genetics|August 30, 1976
Evidence that chromosome band 22q12 is concerned with cell proliferation in chronic myeloid leukaemiaP H Fitzgerald
Human Genetics|August 24, 1999
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathiesR Allikmets, J M Seddon, P S Bernstein, et al.
Human Genetics|August 24, 1999
Gene expression patterns in cell lines from patients with 18q- syndromeZ Wang, J D Cody, R J Leach, et al.
Human Genetics|August 24, 1999
Ancestral origin of variation in the triosephosphate isomerase gene promoterA Humphries, A Ationu, M R Lalloz, et al.
Human Genetics|August 24, 1999
Comparison of complementary and genomic DNA sequencing for the detection of mutations in the HMBS gene in British patients with acute intermittent porphyria: identification of 25 novel mutationsS D Whatley, J R Woolf, G H Elder
Human Genetics|August 24, 1999
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase geneD Pirulli, D Puzzer, L Ferri, et al.
Human Genetics|June 1, 2000
Association of butyrylcholinesterase K variant with cholinesterase-positive neuritic plaques in the temporal cortex in late-onset Alzheimer's diseaseD J Lehmann, Z Nagy, S Litchfield, et al.
Human Genetics|September 15, 2000
Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachyteneE Y Cheng, Y J Chen, C M Disteche, et al.
Pageof 957