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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 families
N 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 obesity
J 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 kidney
M Audebert, S Chevillard, C Levalois, et al.
Nature
|
March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellites
C Dib, S Fauré, C Fizames, et al.
Human Molecular Genetics
|
March 1, 1996
A radiation hybrid map of the human genome
G 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 13q11
A 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 paraplegia
J Hazan, C S Davoine, D Mavel, et al.
Genomics
|
July 8, 1998
A transcriptional Map of the FMF region
A 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 human
J 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 14
J L Escary, E Bottius, N Prince, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 48) with videos related to
Sort By:
Page
of 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 families
N 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 obesity
J 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 kidney
M Audebert, S Chevillard, C Levalois, et al.
Nature
|
March 14, 1996
A comprehensive genetic map of the human genome based on 5,264 microsatellites
C Dib, S Fauré, C Fizames, et al.
Human Molecular Genetics
|
March 1, 1996
A radiation hybrid map of the human genome
G 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 13q11
A 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 paraplegia
J Hazan, C S Davoine, D Mavel, et al.
Genomics
|
July 8, 1998
A transcriptional Map of the FMF region
A 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 human
J 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 14
J L Escary, E Bottius, N Prince, et al.
Page
of 5