Ovarian cancer family and prophylactic choices.

Por Eccles, D M, Houlston, R S
Publicado em 1992

Small cell carcinoma of the oesophagus: report of three cases and review of published cases.

Por Eccles, D M, Allan, S G, Sang, C T, Cornbleet, M A
Publicado em 1989

TP53 intron 6 polymorphism and the risk of ovarian and breast cancer.

Por Mavridou, D., Gornall, R., Campbell, I. G., Eccles, D. M.
Publicado em 1998

BRCA1 polymorphisms.

Por Campbell, I. G., Schroff, R., Englefield, P., Eccles, D. M.
Publicado em 1997

No association of a 306-bp insertion polymorphism in the progesterone receptor gene with ovarian and breast cancer.

Por Manolitsas, T. P., Englefield, P., Eccles, D. M., Campbell, I. G.
Publicado em 1997

BRCA1 mutations in southern England.

Por Eccles, D. M., Englefield, P., Soulby, M. A., Campbell, I. G.
Publicado em 1998

Understanding of BRCA VUS genetic results by breast cancer specialists

Por Eccles, B. K., Copson, E., Maishman, T., Abraham, J. E., Eccles, D. M.
Publicado no BMC Cancer (2015)

Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis.

Por Bunyan, D J, Shea-Simonds, J, Reck, A C, Finnis, D, Eccles, D M
Publicado em 1995

Management of Hereditary Breast Cancer

Por Eccles, D. M., Simmonds, P., Goddards, J., Coultas, M., Lalloo, F., Evans, G., Haites, N.
Publicado em 1999

Overexpression of the p53 protein and allele loss at 17p13 in ovarian carcinoma.

Por Eccles, D. M., Brett, L., Lessells, A., Gruber, L., Lane, D., Steel, C. M., Leonard, R. C.
Publicado em 1992

Minisatellite instability is found in colorectal tumours with mismatch repair deficiency

Por Coleman, M G, Gough, A C, Bunyan, D J, Braham, D, Eccles, D M, Primrose, J N
Publicado em 2001

Cervical intraepithelial neoplasia in lymphoma patients: a cytological and colposcopic study.

Por Hughes, R. G., Colquhoun, M., Eccles, D. M., Alloub, M., Parker, A. C., Norval, M., Smart, G. E.
Publicado em 1989

Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.

Por Barber, J C, Ellis, K H, Bowles, L V, Delhanty, J D, Ede, R F, Male, B M, Eccles, D M
Publicado em 1994

Chromosome 11 allele imbalance and clinicopathological correlates in ovarian tumours.

Por Gabra, H., Taylor, L., Cohen, B. B., Lessels, A., Eccles, D. M., Leonard, R. C., Smyth, J. F., Steel, C. M.
Publicado em 1995

BRCA1 and BRCA2 genetic testing—pitfalls and recommendations for managing variants of uncertain clinical significance

Por Eccles, D. M., Mitchell, G., Monteiro, A. N. A., Schmutzler, R., Couch, F. J., Spurdle, A. B., Gómez-García, E. B.
Publicado no Ann Oncol (2015)

Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene.

Por Eccles, D. M., van der Luijt, R., Breukel, C., Bullman, H., Bunyan, D., Fisher, A., Barber, J., du Boulay, C., Primrose, J., Burn, J., Fodde, R.
Publicado em 1996

Apoptosis, ageing and cancer susceptibility

Por Camplejohn, R S, Gilchrist, R, Easton, D, McKenzie-Edwards, E, Barnes, D M, Eccles, D M, Ardern-Jones, A, Hodgson, S V, Duddy, P M, Eeles, R A
Publicado em 2003

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification

Por Bunyan, D J, Eccles, D M, Sillibourne, J, Wilkins, E, Thomas, N Simon, Shea-Simonds, J, Duncan, P J, Curtis, C E, Robinson, D O, Harvey, J F, Cross, N C P
Publicado em 2004

Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

Por Antoniou, A., Pharoah, P. D. P., Narod, S., Risch, H. A., Eyfjord, J. E., Hopper, J. L., Loman, N., Olsson, H., Johannsson, O., Borg, Å., Pasini, B., Radice, P., Manoukian, S., Eccles, D. M., Tang, N., Olah, E., Anton-Culver, H., Warner, E., Lubinski, J., Gronwald, J., Gorski, B., Tulinius, H., Thorlacius, S., Eerola, H., Nevanlinna, H., Syrjäkoski, K., Kallioniemi, O.-P., Thompson, D., Evans, C., Peto, J., Lalloo, F., Evans, D. G., Easton, D. F.
Publicado em 2003

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

Por Antoniou, A C, Cunningham, A P, Peto, J, Evans, D G, Lalloo, F, Narod, S A, Risch, H A, Eyfjord, J E, Hopper, J L, Southey, M C, Olsson, H, Johannsson, O, Borg, A, Passini, B, Radice, P, Manoukian, S, Eccles, D M, Tang, N, Olah, E, Anton-Culver, H, Warner, E, Lubinski, J, Gronwald, J, Gorski, B, Tryggvadottir, L, Syrjakoski, K, Kallioniemi, O-P, Eerola, H, Nevanlinna, H, Pharoah, P D P, Easton, D F
Publicado em 2008