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Human genetics

Showing results (1091-1100 of 9,569) with videos related to

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Human Genetics|February 23, 1978
Human erythrocyte pyruvate kinase deficiency: the use of a kinetic study of mutant enzymes for the detection of heterozygotesE D Sprengers, J Marie, A Kahn, et al.
Human Genetics|January 1, 1983
Genetic control of adrenergic receptors on human platelets. A twin studyP Propping, W Friedl
Human Genetics|January 1, 1983
DNA restriction mapping identifies the chromosome carrying the mutant Hb Presbyterian beta-globin geneJ Horst, R Oehme, E Kleihauer, et al.
Human Genetics|December 1, 1994
Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisationE Coonen, J C Harper, F C Ramaekers, et al.
Human Genetics|December 1, 1994
The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysisA W Thomas, R Morgan, M Sweeney, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
Human Genetics|December 1, 1994
Exclusion of the cartilage link protein and the cartilage matrix protein genes as the mutant loci in several heritable chondrodysplasiasJ Loughlin, C Irven, B Sykes
Human Genetics|December 1, 1994
Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoaE Chevret, S Rousseaux, M Monteil, et al.
Human Genetics|November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigreesF L Munier, L Arabien, P Flodman, et al.
Human Genetics|November 1, 1994
Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagenN J Rose, K Mackay, A De Paepe, et al.
Pageof 957

Showing results (1091-1100 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|February 23, 1978
Human erythrocyte pyruvate kinase deficiency: the use of a kinetic study of mutant enzymes for the detection of heterozygotesE D Sprengers, J Marie, A Kahn, et al.
Human Genetics|January 1, 1983
Genetic control of adrenergic receptors on human platelets. A twin studyP Propping, W Friedl
Human Genetics|January 1, 1983
DNA restriction mapping identifies the chromosome carrying the mutant Hb Presbyterian beta-globin geneJ Horst, R Oehme, E Kleihauer, et al.
Human Genetics|December 1, 1994
Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisationE Coonen, J C Harper, F C Ramaekers, et al.
Human Genetics|December 1, 1994
The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysisA W Thomas, R Morgan, M Sweeney, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
Human Genetics|December 1, 1994
Exclusion of the cartilage link protein and the cartilage matrix protein genes as the mutant loci in several heritable chondrodysplasiasJ Loughlin, C Irven, B Sykes
Human Genetics|December 1, 1994
Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoaE Chevret, S Rousseaux, M Monteil, et al.
Human Genetics|November 1, 1994
Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigreesF L Munier, L Arabien, P Flodman, et al.
Human Genetics|November 1, 1994
Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagenN J Rose, K Mackay, A De Paepe, et al.
Pageof 957