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Human genetics

Showing results (311-320 of 11,262) with videos related to

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Human Genetics|October 13, 2000
Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21M Guipponi, M L Yaspo, L Riesselman, et al.
Human Genetics|October 13, 2000
Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2)K E Webster, P M Ferree, R P Holmes, et al.
Human Genetics|October 13, 2000
Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate allelesS Castellví-Bel, M Fernández-Burriel, M Rifé, et al.
Human Genetics|October 13, 2000
Genetic association studies of bronchial asthma--a need for Bonferroni correction?S Boehringer, J T Epplen, M Krawczak
Human Genetics|September 12, 2000
Effect of nonsense mutations on PTEN mRNA stabilityA M Raizis, M M Ferguson, P M George
Human Genetics|September 12, 2000
Female fetal cells in maternal blood: use of DNA polymorphisms to prove originO Samura, B Pertl, S Sohda, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|September 12, 2000
Microscopic assessment of pronuclear embryos is not definitiveA S Lim, V H Goh, C L Su, et al.
Human Genetics|September 12, 2000
Variant detection at the delta opioid receptor (OPRD1) locus and population genetics of a novel variant affecting protein sequenceJ Gelernter, H R Kranzler
Human Genetics|September 12, 2000
Fine-mapping of the type 1 diabetes locus (IDDM4) on chromosome 11q and evaluation of two candidate genes (FADD and GALN) by affected sibpair and linkage-disequilibrium analysesS Eckenrode, M P Marron, R Nicholls, et al.
Pageof 1,127

Showing results (311-320 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|October 13, 2000
Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21M Guipponi, M L Yaspo, L Riesselman, et al.
Human Genetics|October 13, 2000
Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2)K E Webster, P M Ferree, R P Holmes, et al.
Human Genetics|October 13, 2000
Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate allelesS Castellví-Bel, M Fernández-Burriel, M Rifé, et al.
Human Genetics|October 13, 2000
Genetic association studies of bronchial asthma--a need for Bonferroni correction?S Boehringer, J T Epplen, M Krawczak
Human Genetics|September 12, 2000
Effect of nonsense mutations on PTEN mRNA stabilityA M Raizis, M M Ferguson, P M George
Human Genetics|September 12, 2000
Female fetal cells in maternal blood: use of DNA polymorphisms to prove originO Samura, B Pertl, S Sohda, et al.
Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.
Human Genetics|September 12, 2000
Microscopic assessment of pronuclear embryos is not definitiveA S Lim, V H Goh, C L Su, et al.
Human Genetics|September 12, 2000
Variant detection at the delta opioid receptor (OPRD1) locus and population genetics of a novel variant affecting protein sequenceJ Gelernter, H R Kranzler
Human Genetics|September 12, 2000
Fine-mapping of the type 1 diabetes locus (IDDM4) on chromosome 11q and evaluation of two candidate genes (FADD and GALN) by affected sibpair and linkage-disequilibrium analysesS Eckenrode, M P Marron, R Nicholls, et al.
Pageof 1,127