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Journal of Medical Genetics
|
September 1, 1995
Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis
D J Bunyan, J Shea-Simonds, A C Reck, et al.
Journal of Medical Genetics
|
June 10, 2011
Prevalence of BRCA1 and BRCA2 mutations in triple negative breast cancer
D G Evans, A Howell, D Ward, et al.
Human Heredity
|
January 1, 1994
Prediction of genetic risks from segregation analyses of morbid risks
D C Shields, A J Marlow, R S Houlston, et al.
Disease Markers
|
December 14, 1999
Management of hereditary breast cancer. European Familial Breast Cancer Collaborative Group
D M Eccles, P Simmonds, J Goddard, et al.
British Journal of Cancer
|
November 27, 2001
Minisatellite instability is found in colorectal tumours with mismatch repair deficiency
M G Coleman, A C Gough, D J Bunyan, et al.
British Journal of Cancer
|
January 1, 1992
Overexpression of the p53 protein and allele loss at 17p13 in ovarian carcinoma
D M Eccles, L Brett, A Lessells, et al.
Annals of Human Genetics
|
May 1, 1997
Segregation analysis of ovarian cancer using diathesis to include other cancers
D M Eccles, P Forabosco, A Williams, et al.
Annals of Clinical Biochemistry
|
March 1, 1993
Alpha-fucosidase as a marker of genetic deletion in ovarian carcinoma
G J Beattie, J E Roulston, D M Eccles, et al.
British Journal of Cancer
|
April 1, 1989
Cervical intraepithelial neoplasia in lymphoma patients: a cytological and colposcopic study
R G Hughes, M Colquhoun, D M Eccles, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1992
A phase I and pharmacology study of GR63178A, a water-soluble analogue of mitoquidone
D M Eccles, J Cummings, M E Stewart, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 6
Journal of Medical Genetics
|
September 1, 1995
Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis
D J Bunyan, J Shea-Simonds, A C Reck, et al.
Journal of Medical Genetics
|
June 10, 2011
Prevalence of BRCA1 and BRCA2 mutations in triple negative breast cancer
D G Evans, A Howell, D Ward, et al.
Human Heredity
|
January 1, 1994
Prediction of genetic risks from segregation analyses of morbid risks
D C Shields, A J Marlow, R S Houlston, et al.
Disease Markers
|
December 14, 1999
Management of hereditary breast cancer. European Familial Breast Cancer Collaborative Group
D M Eccles, P Simmonds, J Goddard, et al.
British Journal of Cancer
|
November 27, 2001
Minisatellite instability is found in colorectal tumours with mismatch repair deficiency
M G Coleman, A C Gough, D J Bunyan, et al.
British Journal of Cancer
|
January 1, 1992
Overexpression of the p53 protein and allele loss at 17p13 in ovarian carcinoma
D M Eccles, L Brett, A Lessells, et al.
Annals of Human Genetics
|
May 1, 1997
Segregation analysis of ovarian cancer using diathesis to include other cancers
D M Eccles, P Forabosco, A Williams, et al.
Annals of Clinical Biochemistry
|
March 1, 1993
Alpha-fucosidase as a marker of genetic deletion in ovarian carcinoma
G J Beattie, J E Roulston, D M Eccles, et al.
British Journal of Cancer
|
April 1, 1989
Cervical intraepithelial neoplasia in lymphoma patients: a cytological and colposcopic study
R G Hughes, M Colquhoun, D M Eccles, et al.
Cancer Chemotherapy and Pharmacology
|
January 1, 1992
A phase I and pharmacology study of GR63178A, a water-soluble analogue of mitoquidone
D M Eccles, J Cummings, M E Stewart, et al.
Page
of 6