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Human genetics

Showing results (491-500 of 11,264) with videos related to

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Human Genetics|November 24, 1978
Differential staining in the secondary constriction regions of human chromosomes A1, C9, and E16 by a heat-hypotonic treatment techniqueN Kanda
Human Genetics|November 24, 1978
Anencephaly in trisomy 18 associated with elevated alpha-1-fetoprotein in amniotic fluidU Merrild, V Schiøler, F Christensen, et al.
Human Genetics|June 1, 1993
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunitM Maekawa, K Sudo, M Kitajima, et al.
Human Genetics|January 1, 1996
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)G Gandon, A M Jouanolle, B Chauvel, et al.
Human Genetics|January 1, 1996
Isolation and characterization of the human mismatch repair gene hMSH2 promoter regionS J Scherer, T Seib, G Seitz, et al.
Human Genetics|January 1, 1996
Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patientsA Savoia, L Ianzano, C Lunardi, et al.
Human Genetics|January 1, 1996
Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha geneH Shapira, M Mouallem, M S Shapiro, et al.
Human Genetics|March 1, 1993
Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridizationJ M Holmes, R H Martin
Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, et al.
Human Genetics|March 1, 1993
Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk populationC Stoll, B Dott, Y Alembik, et al.
Pageof 1,127

Showing results (491-500 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|November 24, 1978
Differential staining in the secondary constriction regions of human chromosomes A1, C9, and E16 by a heat-hypotonic treatment techniqueN Kanda
Human Genetics|November 24, 1978
Anencephaly in trisomy 18 associated with elevated alpha-1-fetoprotein in amniotic fluidU Merrild, V Schiøler, F Christensen, et al.
Human Genetics|June 1, 1993
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunitM Maekawa, K Sudo, M Kitajima, et al.
Human Genetics|January 1, 1996
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)G Gandon, A M Jouanolle, B Chauvel, et al.
Human Genetics|January 1, 1996
Isolation and characterization of the human mismatch repair gene hMSH2 promoter regionS J Scherer, T Seib, G Seitz, et al.
Human Genetics|January 1, 1996
Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patientsA Savoia, L Ianzano, C Lunardi, et al.
Human Genetics|January 1, 1996
Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha geneH Shapira, M Mouallem, M S Shapiro, et al.
Human Genetics|March 1, 1993
Aneuploidy detection in human sperm nuclei using fluorescence in situ hybridizationJ M Holmes, R H Martin
Human Genetics|March 1, 1993
A denaturing gradient gel electrophoresis assay for sensitive detection of p53 mutationsJ S Beck, A E Kwitek, P H Cogen, et al.
Human Genetics|March 1, 1993
Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk populationC Stoll, B Dott, Y Alembik, et al.
Pageof 1,127