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Human genetics

Showing results (821-830 of 9,569) with videos related to

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Human Genetics|February 13, 2003
An Alu-mediated rearrangement as cause of exon skipping in Hunter diseaseVerena Ricci, Stefano Regis, Marco Di Duca, et al.
Human Genetics|May 1, 1993
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11qE C Mariman, S E van Beersum, C W Cremers, et al.
Human Genetics|May 1, 1993
Focal epithelial hyperplasia: human-papillomavirus-induced disease with a genetic predisposition in a Venezuelan familyG Premoli-De-Percoco, J P Cisternas, J L Ramírez, et al.
Human Genetics|July 1, 1993
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformationsS Schneider, G Wildhardt, R Ludwig, et al.
Human Genetics|October 1, 1993
Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissuesB Y Nordvåg, I Ranløv, H M Riise, et al.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Human Genetics|October 1, 1993
Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpointsR J Sinke, B de Leeuw, H A Janssen, et al.
Human Genetics|August 1, 1995
Screening for naturally occurring apolipoprotein A-I variants: apo A-I(delta K107) is associated with low HDL-cholesterol levels in men but not in womenJ R Nofer, A von Eckardstein, H Wiebusch, et al.
Human Genetics|August 1, 1995
Localisation of the human gene encoding the cytoskeletal protein talin to chromosome 9pA P Gilmore, V Ohanian, N K Spurr, et al.
Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
Pageof 957

Showing results (821-830 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|February 13, 2003
An Alu-mediated rearrangement as cause of exon skipping in Hunter diseaseVerena Ricci, Stefano Regis, Marco Di Duca, et al.
Human Genetics|May 1, 1993
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11qE C Mariman, S E van Beersum, C W Cremers, et al.
Human Genetics|May 1, 1993
Focal epithelial hyperplasia: human-papillomavirus-induced disease with a genetic predisposition in a Venezuelan familyG Premoli-De-Percoco, J P Cisternas, J L Ramírez, et al.
Human Genetics|July 1, 1993
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformationsS Schneider, G Wildhardt, R Ludwig, et al.
Human Genetics|October 1, 1993
Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissuesB Y Nordvåg, I Ranløv, H M Riise, et al.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Human Genetics|October 1, 1993
Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpointsR J Sinke, B de Leeuw, H A Janssen, et al.
Human Genetics|August 1, 1995
Screening for naturally occurring apolipoprotein A-I variants: apo A-I(delta K107) is associated with low HDL-cholesterol levels in men but not in womenJ R Nofer, A von Eckardstein, H Wiebusch, et al.
Human Genetics|August 1, 1995
Localisation of the human gene encoding the cytoskeletal protein talin to chromosome 9pA P Gilmore, V Ohanian, N K Spurr, et al.
Human Genetics|August 1, 1995
Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) geneC Mimault, F Cailloux, G Giraud, et al.
Pageof 957