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Human genetics

Showing results (301-310 of 11,262) with videos related to

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Human Genetics|January 1, 1981
Steroid sulphatase levels in XX males, including observations on two affected cousinsP Pierella, I Craig, M Bobrow, et al.
Human Genetics|April 17, 1979
Partial trisomy 6pA Bernheim, R Berger, G Vaugier, et al.
Human Genetics|November 9, 2000
Compound heterozygosity for two different amino-acid substitution mutations in the thrombopoietin receptor (c-mpl gene) in congenital amegakaryocytic thrombocytopenia (CAMT)R Tonelli, A L Scardovi, A Pession, et al.
Human Genetics|November 9, 2000
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancerF Krämer, K White, M Kubbies, et al.
Human Genetics|November 9, 2000
Genetic screening of the lipoprotein lipase gene for mutations associated with high triglyceride/low HDL-cholesterol levelsH Razzaghi, C E Aston, R F Hamman, et al.
Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.
Human Genetics|October 30, 1999
Beta3-adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study. Atherosclerosis Risk in CommunitiesA C Morrison, F L Brancati, A R Folsom, et al.
Human Genetics|October 30, 1999
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutationsM J Osborn, M Upadhyaya
Human Genetics|October 30, 1999
Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor geneC Cybulski, K Krzystolik, E R Maher, et al.
Human Genetics|October 13, 2000
Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesisM Koptides, C C Deltas
Pageof 1,127

Showing results (301-310 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|January 1, 1981
Steroid sulphatase levels in XX males, including observations on two affected cousinsP Pierella, I Craig, M Bobrow, et al.
Human Genetics|April 17, 1979
Partial trisomy 6pA Bernheim, R Berger, G Vaugier, et al.
Human Genetics|November 9, 2000
Compound heterozygosity for two different amino-acid substitution mutations in the thrombopoietin receptor (c-mpl gene) in congenital amegakaryocytic thrombocytopenia (CAMT)R Tonelli, A L Scardovi, A Pession, et al.
Human Genetics|November 9, 2000
Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancerF Krämer, K White, M Kubbies, et al.
Human Genetics|November 9, 2000
Genetic screening of the lipoprotein lipase gene for mutations associated with high triglyceride/low HDL-cholesterol levelsH Razzaghi, C E Aston, R F Hamman, et al.
Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.
Human Genetics|October 30, 1999
Beta3-adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study. Atherosclerosis Risk in CommunitiesA C Morrison, F L Brancati, A R Folsom, et al.
Human Genetics|October 30, 1999
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutationsM J Osborn, M Upadhyaya
Human Genetics|October 30, 1999
Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor geneC Cybulski, K Krzystolik, E R Maher, et al.
Human Genetics|October 13, 2000
Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesisM Koptides, C C Deltas
Pageof 1,127