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Cytogenetics and Cell Genetics
|
January 1, 1988
Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy
K J Johnson, P J Jones, N Spurr, et al.
The British Journal of Dermatology
|
April 1, 1988
Plasma 5-S-cysteinyldopa as an index of melanogenesis
J E Nimmo, D J Gawkrodger, C S O'Docherty, et al.
Genomics
|
November 1, 1989
Recombination events that locate myotonic dystrophy distal to APOC2 on 19q
K Johnson, P Shelbourne, J Davies, et al.
American Journal of Human Genetics
|
June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus
K Johnson, P Shelbourne, J Davies, et al.
Human Genetics
|
December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q
K Johnson, E Nimmo, P Jones, et al.
Alimentary Pharmacology & Therapeutics
|
January 16, 2008
Low body mass not vitamin D receptor polymorphisms predict osteoporosis in patients with inflammatory bowel disease
C L Noble, J McCullough, W Ho, et al.
Inflammatory Bowel Diseases
|
October 22, 2005
Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease
Richard K Russell, Hazel E Drummond, Elaine E Nimmo, et al.
Nature Communications
|
August 10, 2016
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Manuel A Rivas, Daniel Graham, Patrick Sulem, et al.
QJM : Monthly Journal of the Association of Physicians
|
June 22, 2019
Scientific Business Abstracts of the 112th Annual Meeting of the Association of Physicians of Great Britain and Ireland
A Chauhan, T Lalor, S Watson, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Cytogenetics and Cell Genetics
|
January 1, 1988
Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy
K J Johnson, P J Jones, N Spurr, et al.
The British Journal of Dermatology
|
April 1, 1988
Plasma 5-S-cysteinyldopa as an index of melanogenesis
J E Nimmo, D J Gawkrodger, C S O'Docherty, et al.
Genomics
|
November 1, 1989
Recombination events that locate myotonic dystrophy distal to APOC2 on 19q
K Johnson, P Shelbourne, J Davies, et al.
American Journal of Human Genetics
|
June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus
K Johnson, P Shelbourne, J Davies, et al.
Human Genetics
|
December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q
K Johnson, E Nimmo, P Jones, et al.
Alimentary Pharmacology & Therapeutics
|
January 16, 2008
Low body mass not vitamin D receptor polymorphisms predict osteoporosis in patients with inflammatory bowel disease
C L Noble, J McCullough, W Ho, et al.
Inflammatory Bowel Diseases
|
October 22, 2005
Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease
Richard K Russell, Hazel E Drummond, Elaine E Nimmo, et al.
Nature Communications
|
August 10, 2016
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Manuel A Rivas, Daniel Graham, Patrick Sulem, et al.
QJM : Monthly Journal of the Association of Physicians
|
June 22, 2019
Scientific Business Abstracts of the 112th Annual Meeting of the Association of Physicians of Great Britain and Ireland
A Chauhan, T Lalor, S Watson, et al.
Page
of 2