Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy

Por West, P, Love, D, Stapleton, P, Winship, I
Publicado em 2003

Genetic heterogeneity in tuberous sclerosis: phenotypic correlations.

Por Winship, I M, Connor, J M, Beighton, P H
Publicado em 1990

Improving the provision of Melbourne Health Familial Cancer services to Victoria’s Culturally and Linguistically Diverse (CALD) communities

Por Bylstra, Y, Kentwell, M, Lindeman, GJ, Winship, I, Hodgkin, L
Publicado em 2012

Autosomal translocation associated with premature ovarian failure

Por BURTON, K., VAN EE, C. C, PURCELL, K., WINSHIP, I., SHELLING, A.
Publicado em 2000

Microcephaly-cardiomyopathy: a new autosomal recessive phenotype?

Por Winship, I M, Viljoen, D L, Leary, P M, De Moor, M M
Publicado em 1991

What are the unmet support needs of women with a known BRCA1/2 mutation?

Por White, V, Farrelly, A, Meiser, B, Jefford, M, Young, M, Winship, I, Ieropoli, S, Koehler, J
Publicado em 2012

DNA microsatellite instability and mismatch repair protein loss in adenomas presenting in hereditary non-polyposis colorectal cancer

Por Iino, H, Simms, L, Young, J, Arnold, J, Winship, I, Webb, S, Furlong, K, Leggett, B, Jass, J
Publicado em 2000

Evidence for genetic heterogeneity in tuberous sclerosis.

Por Sampson, J R, Yates, J R, Pirrit, L A, Fleury, P, Winship, I, Beighton, P, Connor, J M
Publicado em 1989

P-236 Screening practices of Australians at population and familial risk following the partial roll-out of the National Bowel Cancer Screening Program, 2009-2012

Por Flander, L., Jenkins, M., Win Aung, K., Boussioutas, A., Hopper, J., Giles, G., Winship, I., Macrae, F., Ait Ouakrim, D.
Publicado no Ann Oncol (2016)

Peer live supervision in the familial cancer setting

Por Kentwell, M, Sexton, A, Hodgkin, L, Bylstra, Y, Bogwitz, M, Mann, K, Taylor, J, Sahhar, M, Pearce, F, Winship, I, Lindeman, GJ
Publicado em 2012

X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats.

Por Bassi, M T, Ramesar, R S, Caciotti, B, Winship, I M, De Grandi, A, Riboni, M, Townes, P L, Beighton, P, Ballabio, A, Borsani, G
Publicado em 1999

Expanded genetic analysis of a PALB2 c.3113G>A mutation carrying multiple-case breast cancer family via exome sequencing

Por Teo, ZL, Park, DJ, Odefrey, F, Hammet, F, Nguyen-Dumont, T, Tsimiklis, H, Pope, BJ, Lonie, A, Winship, I, Giles, GG, Hopper, JL, Southey, MC
Publicado em 2012

Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities.

Por Dunnill, M G, Richards, A J, Milana, G, Mollica, F, Atherton, D, Winship, I, Farrall, M, al-Imara, L, Eady, R A, Pope, F M
Publicado em 1994

Appreciating the broad clinical features of SMAD4 mutation carriers: a multi-center chart review

Por Wain, K.E., Ellingson, M.S., McDonald, J., Gammon, A., Roberts, M., Pichurin, P., Winship, I., Riegert-Johnson, D., Weitzel, J. N., Lindor, N.M.
Publicado em 2014

Analysis of the TGFβ functional pathway in epithelial ovarian carcinoma

Por Francis-Thickpenny, K M, Richardson, D M, Ee, C C van, Love, D R, Winship, I M, Baguley, B C, Chenevix-Trench, G, Shelling, A N
Publicado em 2001

Morphological predictors of BRCA1 germline mutations in young women with breast cancer

Por Southey, M C, Ramus, S J, Dowty, J G, Smith, L D, Tesoriero, A A, Wong, E E M, Dite, G S, Jenkins, M A, Byrnes, G B, Winship, I, Phillips, K-A, Giles, G G, Hopper, J L
Publicado em 2011

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

Por Win, A K, Dowty, J G, English, D R, Campbell, P T, Young, J P, Winship, I, Macrae, F A, Lipton, L, Parry, S, Young, G P, Buchanan, D D, Martínez, M E, Jacobs, E T, Ahnen, D J, Haile, R W, Casey, G, Baron, J A, Lindor, N M, Thibodeau, S N, Newcomb, P A, Potter, J D, Le Marchand, L, Gallinger, S, Hopper, J L, Jenkins, M A
Publicado em 2011

Tumour morphology predicts PALB2 germline mutation status

Por Teo, Z L, Provenzano, E, Dite, G S, Park, D J, Apicella, C, Sawyer, S D, James, P A, Mitchell, G, Trainer, A H, Lindeman, G J, Shackleton, K, Cicciarelli, L, Buys, S S, Andrulis, I L, Mulligan, A M, Glendon, G, John, E M, Terry, M B, Daly, M, Odefrey, F A, Nguyen-Dumont, T, Giles, G G, Dowty, J G, Winship, I, Goldgar, D E, Hopper, J L, Southey, M C
Publicado em 2013