Preoperative Diagnosis of Lynch Syndrome With DNA Mismatch Repair Immunohistochemistry on a Diagnostic Biopsy von Warrier, S. K, Trainer, A. H, Lynch, A. C, Mitchell, C, Hiscock, R, Sawyer, S, Boussioutas, A, Heriot, A. G

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Familial colorectal cancer von Lung, M. S., Trainer, A. H., Campbell, I., Lipton, L.

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Clinical studies on submicroscopic subtelomeric rearrangements: a checklist von de Vries, B B A, White, S M, Knight, S J L, Regan, R, Homfray, T, Young, I D, Super, M, McKeown, C, Splitt, M, Quarrell, O W J, Trainer, A H, Niermeijer, M F, Malcolm, S, Flint, J, Hurst, J A, Winter, R M

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Tumour morphology predicts PALB2 germline mutation status von 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

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Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same von Huq, A. J., Walsh, M., Rajagopalan, B., Finlay, M., Trainer, A. H., Bonnet, F., Sevenet, N., Winship, I. M.

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Consumer and clinician perspectives on personalising breast cancer prevention information von Keogh, L.A., Steel, E., Weideman, P., Butow, P., Collins, I.M., Emery, J.D., Mann, G.B., Bickerstaffe, A., Trainer, A.H., Hopper, L.J., Phillips, K.A.

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Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics von Meiser, B., Kaur, R., Kirk, J., Morrow, A., Peate, M., Wong, W. K. T., McPike, E., Cops, E., Dowson, C., Austin, R., Fine, M., Thrupp, L., Ward, R., Macrae, F., Hiller, J. E., Trainer, A. H., Mitchell, G.

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Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes... von Vega, H, Trainer, A H, Gordillo, M, Crosier, M, Kayserili, H, Skovby, F, Uzielli, M L Giovannucci, Schnur, R E, Manouvrier, S, Blair, E, Hurst, J A, Forzano, F, Meins, M, Simola, K O J, Raas-Rothschild, A, Hennekam, R C M, Jabs, E Wang

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Rothmund–Thomson Syndrome with Myelodysplasia von Narayan, S., Fleming, C., Trainer, A. H., Craig, J. A.

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A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation von Ghaffari, S R, Boyd, E, Tolmie, J L, Crow, Y J, Trainer, A H, Connor, J M

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Mitotic Checkpoint Inactivation Fosters Transformation in Cells Lacking the Breast Cancer Susceptibility Gene, Brca2 von Lee, Hyunsook, Trainer, Alison H, Friedman, Lori S, Thistlethwaite, Fiona C, Evans, Martin J, Ponder, Bruce A.J, Venkitaraman, Ashok R

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Chromosome 22q11 microdeletions in tetralogy of Fallot von Trainer, A H, Morrison, N, Dunlop, A, Wilson, N, Tolmie, J

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Gene Delivery to the Epidermis von Trainer, Alison H., Alexander, M. Yvonne

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Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same: Fam Cancer von Huq, A. J., Walsh, M., Rajagopalan, B., Finlay, M., Trainer, A. H., Bonnet, Fabrice, Sevenet, N., Winship, I. M.

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Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients von Thompson, ER, Boyle, SE, Johnson, J, Ryland, GL, Sawyer, S, Choong, DY, Chenevix-Trench, G, Trainer, AH, Lindeman, GJ, Mitchell, G, James, PA, Campbell, IG

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An Economic Evaluation of a Familial Cancer Risk Management Program for Brca Mutation Carriers: An Australian Perspective von Petelin, L, Liew, D, Mitchell, G, James, PA, Trainer, AH

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CE4 - An Economic Evaluation of a Familial Cancer Risk Management Program for Brca Mutation Carriers: An Australian Perspective von Petelin, L, Liew, D, Mitchell, G, James, PA, Trainer, AH

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Abstract P2-02-01: Identifying the remaining causes of hereditary breast cancer von Campbell, IG, Trainer, AH, Devereux, L, James, PA, Rowley, S, Li, N

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Abstract P2-09-03: Breast cancer prevention: Is it time for population-based mutation screening of high risk genes? von Campbell, IG, Trainer, AH, Devereux, L, Young, M-A, Mitchell, G, Rowley, S, Li, N, James, PA, Thompson, E

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Abstract P2-09-02: Panel testing for familial breast cancer: Tension at the boundary of research and clinical care von Campbell, IG, Thompson, ER, Rowely, SM, Li, N, McInerny, S, Devereux, L, Wong-Brown, MW, Trainer, AH, Mitchell, G, Scott, RJ, James, PA

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