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British Journal of Cancer
|
March 10, 1999
Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions
A Catteau, C F Xu, M A Brown, et al.
American Journal of Human Genetics
|
April 1, 1994
Mutation analysis of the Fanconi anemia gene FACC
P C Verlander, J D Lin, M U Udono, et al.
Pediatric Blood & Cancer
|
December 14, 2004
Nijmegen breakage syndrome diagnosed as Fanconi anaemia
Helen V New, C M Cale, M Tischkowitz, et al.
Annals of Human Genetics
|
May 1, 1990
Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping
C G Mathew, W Wakeling, E Jones, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy
J E Taylor, N H Thomas, C M Lewis, et al.
Genes and Immunity
|
May 26, 2006
Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31
C Onnie, S A Fisher, K King, et al.
Nucleic Acids Research
|
September 26, 1988
BclI RFLP for the human vimentin gene
E M Marcus, B A Smith, H Telenius, et al.
Tissue Antigens
|
September 28, 2005
A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population
N J Prescott, S A Fisher, C Onnie, et al.
Rheumatology (Oxford, England)
|
February 22, 2003
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15
S Steer, S A Fisher, M Fife, et al.
Journal of Medical Genetics
|
January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXE
A J Barnicoat, Q Wang, J Turk, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 129) with videos related to
Sort By:
Page
of 13
British Journal of Cancer
|
March 10, 1999
Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions
A Catteau, C F Xu, M A Brown, et al.
American Journal of Human Genetics
|
April 1, 1994
Mutation analysis of the Fanconi anemia gene FACC
P C Verlander, J D Lin, M U Udono, et al.
Pediatric Blood & Cancer
|
December 14, 2004
Nijmegen breakage syndrome diagnosed as Fanconi anaemia
Helen V New, C M Cale, M Tischkowitz, et al.
Annals of Human Genetics
|
May 1, 1990
Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping
C G Mathew, W Wakeling, E Jones, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy
J E Taylor, N H Thomas, C M Lewis, et al.
Genes and Immunity
|
May 26, 2006
Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31
C Onnie, S A Fisher, K King, et al.
Nucleic Acids Research
|
September 26, 1988
BclI RFLP for the human vimentin gene
E M Marcus, B A Smith, H Telenius, et al.
Tissue Antigens
|
September 28, 2005
A general autoimmunity gene (PTPN22) is not associated with inflammatory bowel disease in a British population
N J Prescott, S A Fisher, C Onnie, et al.
Rheumatology (Oxford, England)
|
February 22, 2003
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15
S Steer, S A Fisher, M Fife, et al.
Journal of Medical Genetics
|
January 1, 1997
Clinical, cytogenetic, and molecular analysis of three families with FRAXE
A J Barnicoat, Q Wang, J Turk, et al.
Page
of 13