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Human genetics

Showing results (831-840 of 9,569) with videos related to

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Human Genetics|August 1, 1995
A novel polymorphism (6376 G/T) in intron 7 of the human protein C geneJ M Soria, M Morell, X Estivill, et al.
Human Genetics|February 1, 1993
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridizationS du Manoir, M R Speicher, S Joos, et al.
Human Genetics|February 1, 1993
A single amino acid deletion in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type IIIK Molyneux, B J Starman, P H Byers, et al.
Human Genetics|February 1, 1993
An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphismN Dalla Venezia, R Wilmotte, L Morlé, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Human Genetics|February 1, 1993
A sequence variation in the human cystatin D gene resulting in an amino acid (Cys/Arg) polymorphism at the protein levelM Balbín, J P Freije, M Abrahamson, et al.
Human Genetics|February 11, 1977
A photometric method for quantifying the polymorphisms in human acrocentric chromosomesW Schnedl, U Roscher, R Czaker
Human Genetics|February 11, 1977
Differential chromosomal radiosensitivity within the first G1-phase of the cell cycle of early-dividing human leukocytes in vitro after stimulation with PHAB Beek, G Obe
Human Genetics|April 1, 1993
Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern QuebecM De Braekeleer, A Dallaire, J Mathieu
Human Genetics|April 1, 1993
The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastomaJ A Byrne, P J Smith
Pageof 957

Showing results (831-840 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|August 1, 1995
A novel polymorphism (6376 G/T) in intron 7 of the human protein C geneJ M Soria, M Morell, X Estivill, et al.
Human Genetics|February 1, 1993
Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridizationS du Manoir, M R Speicher, S Joos, et al.
Human Genetics|February 1, 1993
A single amino acid deletion in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type IIIK Molyneux, B J Starman, P H Byers, et al.
Human Genetics|February 1, 1993
An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphismN Dalla Venezia, R Wilmotte, L Morlé, et al.
Human Genetics|February 1, 1993
Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeA Moncla, L Piras, O F Arbex, et al.
Human Genetics|February 1, 1993
A sequence variation in the human cystatin D gene resulting in an amino acid (Cys/Arg) polymorphism at the protein levelM Balbín, J P Freije, M Abrahamson, et al.
Human Genetics|February 11, 1977
A photometric method for quantifying the polymorphisms in human acrocentric chromosomesW Schnedl, U Roscher, R Czaker
Human Genetics|February 11, 1977
Differential chromosomal radiosensitivity within the first G1-phase of the cell cycle of early-dividing human leukocytes in vitro after stimulation with PHAB Beek, G Obe
Human Genetics|April 1, 1993
Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern QuebecM De Braekeleer, A Dallaire, J Mathieu
Human Genetics|April 1, 1993
The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastomaJ A Byrne, P J Smith
Pageof 957