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G Gyapay

Showing results (31-40 of 48) with videos related to

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American Journal of Human Genetics|May 1, 1995
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 familiesN Doerflinger, C Linder, K Ouahchi, et al.
International Journal of Obesity (2005)|June 4, 2014
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesityJ Philippe, P Stijnen, D Meyre, et al.
Cancer Research|September 15, 2000
Alterations of the DNA repair gene OGG1 in human clear cell carcinomas of the kidneyM Audebert, S Chevillard, C Levalois, et al.
Nature|March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellitesC Dib, S Fauré, C Fizames, et al.
Human Molecular Genetics|March 1, 1996
A radiation hybrid map of the human genomeG Gyapay, K Schmitt, C Fizames, et al.
American Journal of Human Genetics|March 3, 1999
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11A Richter, J D Rioux, J P Bouchard, et al.
Genomics|September 24, 1999
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegiaJ Hazan, C S Davoine, D Mavel, et al.
Genomics|July 8, 1998
A transcriptional Map of the FMF regionA Bernot, R Heilig, C Clepet, et al.
Genomics|March 15, 1996
Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and humanJ A Tischfield, Y R Xia, D M Shih, et al.
Genomics|December 9, 2000
A first high-density map of 981 biallelic markers on human chromosome 14J L Escary, E Bottius, N Prince, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|May 1, 1995
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 familiesN Doerflinger, C Linder, K Ouahchi, et al.
International Journal of Obesity (2005)|June 4, 2014
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesityJ Philippe, P Stijnen, D Meyre, et al.
Cancer Research|September 15, 2000
Alterations of the DNA repair gene OGG1 in human clear cell carcinomas of the kidneyM Audebert, S Chevillard, C Levalois, et al.
Nature|March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellitesC Dib, S Fauré, C Fizames, et al.
Human Molecular Genetics|March 1, 1996
A radiation hybrid map of the human genomeG Gyapay, K Schmitt, C Fizames, et al.
American Journal of Human Genetics|March 3, 1999
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11A Richter, J D Rioux, J P Bouchard, et al.
Genomics|September 24, 1999
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegiaJ Hazan, C S Davoine, D Mavel, et al.
Genomics|July 8, 1998
A transcriptional Map of the FMF regionA Bernot, R Heilig, C Clepet, et al.
Genomics|March 15, 1996
Low-molecular-weight, calcium-dependent phospholipase A2 genes are linked and map to homologous chromosome regions in mouse and humanJ A Tischfield, Y R Xia, D M Shih, et al.
Genomics|December 9, 2000
A first high-density map of 981 biallelic markers on human chromosome 14J L Escary, E Bottius, N Prince, et al.
Pageof 5