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Human genetics

Showing results (911-920 of 9,569) with videos related to

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Human Genetics|September 1, 1996
CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern FranceM Claustres, M Desgeorges, P Moine, et al.
Human Genetics|September 1, 1996
Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German familyJ Bürger, H Metzke, C Paternotte, et al.
Human Genetics|August 1, 1996
Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophyS Ishii, T Nishio, N Sunohara, et al.
Human Genetics|August 1, 1996
Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genesB D Gelb, E Spencer, S Obad, et al.
Human Genetics|August 1, 1996
Geographic homogeneity and non-equilibrium patterns of mtDNA sequences in Tuscany, ItalyG Bertorelle, F Calafell, P Francalacci, et al.
Human Genetics|August 1, 1996
Analysis of sex and delta F508 in single amniocytes using primer extension preamplificationF Schaaff, H Wedemann, E Schwinger
Human Genetics|August 1, 1996
Fetal cells in maternal blood: recovery by charge flow separationS S Wachtel, D Sammons, M Manley, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
Human Genetics|August 1, 1996
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs alpha geneL DeMarco, C A Stratakis, W L Boson, et al.
Pageof 957

Showing results (911-920 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|September 1, 1996
CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern FranceM Claustres, M Desgeorges, P Moine, et al.
Human Genetics|September 1, 1996
Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German familyJ Bürger, H Metzke, C Paternotte, et al.
Human Genetics|August 1, 1996
Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophyS Ishii, T Nishio, N Sunohara, et al.
Human Genetics|August 1, 1996
Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genesB D Gelb, E Spencer, S Obad, et al.
Human Genetics|August 1, 1996
Geographic homogeneity and non-equilibrium patterns of mtDNA sequences in Tuscany, ItalyG Bertorelle, F Calafell, P Francalacci, et al.
Human Genetics|August 1, 1996
Analysis of sex and delta F508 in single amniocytes using primer extension preamplificationF Schaaff, H Wedemann, E Schwinger
Human Genetics|August 1, 1996
Fetal cells in maternal blood: recovery by charge flow separationS S Wachtel, D Sammons, M Manley, et al.
Human Genetics|August 1, 1996
X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 geneC Ressot, P Latour, F Blanquet-Grossard, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
Human Genetics|August 1, 1996
Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gs alpha geneL DeMarco, C A Stratakis, W L Boson, et al.
Pageof 957