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Human genetics

Showing results (761-770 of 9,569) with videos related to

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Human Genetics|February 22, 2023
Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulinMd Rafiqul Islam, , Dale R Nyholt
Human Genetics|February 11, 2023
Phenome-wide genetic-correlation analysis and genetically informed causal inference of amyotrophic lateral sclerosisSalvatore D'Antona, Gita A Pathak, Dora Koller, et al.
Human Genetics|December 18, 1978
Demonstration of replication patterns corresponding to G- and R-type banding of chromosomes after partial synchronization of cell cultures with BrdU or dT surplusW Schempp, I Sigwarth, W Vogel
Human Genetics|April 6, 1999
World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological markerG Pepe, O C Vanegas, O Rickards, et al.
Human Genetics|April 3, 2001
Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7D Balmer, J M LaSalle
Human Genetics|April 3, 2001
Lack of association between alpha2-macroglobulin polymorphisms and Alzheimer's diseaseX Wang, E K Luedecking, R L Minster, et al.
Human Genetics|April 3, 2001
Neonatal presentation of adult-onset type II citrullinemiaT Ohura, K Kobayashi, Y Tazawa, et al.
Human Genetics|April 3, 2001
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variantsK M Boycott, T A Maybaum, M J Naylor, et al.
Human Genetics|April 4, 2000
Genetics of molybdenum cofactor deficiencyJ Reiss
Human Genetics|April 4, 2000
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridizationL Voullaire, H Slater, R Williamson, et al.
Pageof 957

Showing results (761-770 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|February 22, 2023
Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulinMd Rafiqul Islam, , Dale R Nyholt
Human Genetics|February 11, 2023
Phenome-wide genetic-correlation analysis and genetically informed causal inference of amyotrophic lateral sclerosisSalvatore D'Antona, Gita A Pathak, Dora Koller, et al.
Human Genetics|December 18, 1978
Demonstration of replication patterns corresponding to G- and R-type banding of chromosomes after partial synchronization of cell cultures with BrdU or dT surplusW Schempp, I Sigwarth, W Vogel
Human Genetics|April 6, 1999
World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological markerG Pepe, O C Vanegas, O Rickards, et al.
Human Genetics|April 3, 2001
Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7D Balmer, J M LaSalle
Human Genetics|April 3, 2001
Lack of association between alpha2-macroglobulin polymorphisms and Alzheimer's diseaseX Wang, E K Luedecking, R L Minster, et al.
Human Genetics|April 3, 2001
Neonatal presentation of adult-onset type II citrullinemiaT Ohura, K Kobayashi, Y Tazawa, et al.
Human Genetics|April 3, 2001
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variantsK M Boycott, T A Maybaum, M J Naylor, et al.
Human Genetics|April 4, 2000
Genetics of molybdenum cofactor deficiencyJ Reiss
Human Genetics|April 4, 2000
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridizationL Voullaire, H Slater, R Williamson, et al.
Pageof 957