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Results 1-10 of 18 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2000
Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Barratt, A.
;
Suthers, G.
;
Smith, M.
;
Colley, A.
;
Thompson, E.
;
Tucker, K.
1997
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident
Wicking, C.
;
Shanley, S.
;
Smyth, I.
;
Gillies, S.
;
Negus, K.
;
Graham, S.
;
Suthers, G.
;
Haites, N.
;
Edwards, M.
;
Wainwright, B.
;
Chenevix Trench, G.
2001
A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers
Wang, W.
;
Spurdle, A.
;
Kolachana, P.
;
Bove, B.
;
Modan, B.
;
Ebbers, S.
;
Suthers, G.
;
Tucker, M.
;
Kaufman, D.
;
Doody, M.
;
Tarone, R.
;
Daly, M.
;
Levavi, H.
;
Pierce, H.
;
Chetrit, A.
;
Yechezkel, G.
;
Chenevix-Trench, G.
;
Offit, K.
;
Godwin, A.
;
Struewing, J.
2000
New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome
Cox, T.
;
Allen, L.
;
Cox, L.
;
Hopwood, B.
;
Goodwin, B.
;
Haan, E.
;
Suthers, G.
2000
Intention to undergo prophylactic bilateral mastectomy in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Friedlander, M.
;
Schnieden, V.
;
Gattas, M.
;
Kirk, J.
;
Suthers, G.
;
Haan, E.
;
Tucker, K.
1997
Mutation detection in FGFR2 craniosynostosis syndromes
Hollway, G.
;
Suthers, G.
;
Haan, E.
;
Thompson, E.
;
David, D.
;
Gecz, J.
;
Mulley, J.
2005
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers
Chenevix-Trench, G.
;
Sinilnikova, O.
;
Suthers, G.
;
Pandeya, N.
;
Mazoyer, S.
;
Sambrook, J.
;
Goldup, S.
;
Goldgar, D.
;
Lynch, H.
;
Lenoir, G.
;
Cheetham, G.
2001
Long-term outcomes of genetic counseling in women at increased risk of developing hereditary breast cancer
Meiser, B.
;
Butow, P.
;
Barratt, A.
;
Schneiden, V.
;
Gattas, M.
;
Kirk, J.
;
Gaff, C.
;
Suthers, G.
;
Tucker, K.
2010
Risks of Lynch Syndrome cancers for MSH6 mutation carriers
Suthers, G.
2000
Microsatellite instability markers in breast cancer: A review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancer
Siah, S.
;
Quinn, D.
;
Bennet, G.
;
Casey, G.
;
Flower, R.
;
Suthers, G.
;
Rudzki, Z.
Discover
Author
4
Tucker, K.
3
Butow, P.
3
Chenevix-Trench, G.
3
Gattas, M.
3
Haan, E.
3
Kirk, J.
3
Meiser, B.
2
Barratt, A.
2
Goldblatt, J.
2
Hawkins, N.
.
next >
Subject
18
Humans
13
Adult
13
Middle Aged
10
Male
9
Aged
9
Breast Neoplasms
7
Pedigree
6
Genetic Predisposition to Disease
5
Australia
5
Colorectal Neoplasms, Hereditary ...
.
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Date issued
4
2010 - 2012
12
2000 - 2009
2
1997 - 1999