Search research articles
Contact Us
Filters
Showing results (121-130 of 129) with videos related to
Page
of 13
Sort By:
You have reached the last page of results.
This site can display upto 129 results.
Genomics
|
June 20, 1998
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer
S A Whitmore, J Crawford, S Apostolou, et al.
Lancet (London, England)
|
June 27, 2001
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
J Hampe, A Cuthbert, P J Croucher, et al.
American Journal of Human Genetics
|
March 3, 1999
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
J Hampe, S Schreiber, S H Shaw, et al.
Genomics
|
October 29, 1998
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
S A Whitmore, C Settasatian, J Crawford, et al.
Blood
|
December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group
L Faivre, P Guardiola, C Lewis, et al.
American Journal of Human Genetics
|
September 23, 2000
Isolation of a cDNA representing the Fanconi anemia complementation group E gene
J P de Winter, F Léveillé, C G van Berkel, et al.
Human Mutation
|
January 1, 1996
Novel mutations and polymorphisms in the Fanconi anemia group C gene
R A Gibson, N V Morgan, L H Goldstein, et al.
Mucosal Immunology
|
November 2, 2017
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease
T Schwerd, R V Bryant, S Pandey, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
September 16, 2017
International cancer seminars: a focus on esophageal squamous cell carcinoma
G Murphy, V McCormack, B Abedi-Ardekani, et al.
Page
of 13
Search research articles
Search
Showing results (121-130 of 129) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 129 results.
Genomics
|
June 20, 1998
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer
S A Whitmore, J Crawford, S Apostolou, et al.
Lancet (London, England)
|
June 27, 2001
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
J Hampe, A Cuthbert, P J Croucher, et al.
American Journal of Human Genetics
|
March 3, 1999
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
J Hampe, S Schreiber, S H Shaw, et al.
Genomics
|
October 29, 1998
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
S A Whitmore, C Settasatian, J Crawford, et al.
Blood
|
December 9, 2000
Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group
L Faivre, P Guardiola, C Lewis, et al.
American Journal of Human Genetics
|
September 23, 2000
Isolation of a cDNA representing the Fanconi anemia complementation group E gene
J P de Winter, F Léveillé, C G van Berkel, et al.
Human Mutation
|
January 1, 1996
Novel mutations and polymorphisms in the Fanconi anemia group C gene
R A Gibson, N V Morgan, L H Goldstein, et al.
Mucosal Immunology
|
November 2, 2017
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease
T Schwerd, R V Bryant, S Pandey, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
September 16, 2017
International cancer seminars: a focus on esophageal squamous cell carcinoma
G Murphy, V McCormack, B Abedi-Ardekani, et al.
Page
of 13