Hereditary Cancer in Clinical Practice

Title Publication Date Language Citations
An incidental finding of a large genomic deletion of BRCA1 on a molecular karyotype for a 5 year old child2012/01/01English
Bowel cancer chemoprevention - ready for the clinic?2012/01/01English
Selecting women for breast cancer chemoprevention and what agents should be used2012/01/01English
Making a good model better - evaluation of the NSW Combined Family Cancer Clinic meetings2012/01/01English
Pathogenic germline TP53 mutations in adult sarcoma patients; implications for treatment and screening – description of an upcoming project2012/01/01English
Rehabilitating the sick role: post-surgical experiences of high risk women who undergo risk reducing mastectomy2012/01/01English
Chemoprevention with the metabolism modifying drugs dichloroacetate and metformin in Trp53+/- mice2012/01/01English
Are women at high risk for serous gynaecological cancer (SGC) opting for risk-reducing salphingo-oophorectomy motivated by high levels of anxiety and risk perceptions?2012/01/01English
The relationship between the BRAF p.V600E mutation and a family history of CRC in the early-onset CRC cases from the Australasian Colon Cancer Family Study2012/01/01English
Integrated genomic analysis and functional characterisation of novel oncogenes in ovarian cancer2012/01/01English
Contribution of genetic variation within SuprMam1 and SuprMam2 to breast cancer susceptibility2012/01/01English
Inherited and de novo germline TP53 mutations in adult-onset sarcoma2012/01/01English
Improving the provision of Melbourne Health Familial Cancer services to Victoria’s Culturally and Linguistically Diverse (CALD) communities2012/01/01English
Bowel cancer in a 17 year old: what could be the reason?2012/01/01English
Genetic testing and immunohistochemistry for SDHB in phaeochromocytoma-paraganglioma syndromes: the South Australian experience2012/01/01English
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients2012/01/01English
Identification of breast cancer susceptibility genes using whole exome sequencing2012/01/01English
An audit of families with unreported or misreported cancers verified through a population-based cancer registry: implications for providing cancer risk assessment and management advice by a Familial Cancer Centre2012/01/01English
Metachronous colon cancer risk following surgery for first primary rectal cancer in Lynch syndrome2012/01/01English
An audit of treatment focussed BRCA1/2 mutation testing at an integrated Familial Cancer Clinic2012/01/01English
Hyperplastic polyposis syndrome: endoscopic imaging, phenotypic charcteristics and molecular pathways2012/01/01English
Loss of MSH6 and PMS2 immunohistochemical staining in tumour tissue of two individuals with a germline PMS2 mutation2012/01/01English
I just did it for the kids: mothering in the context of living with an increased risk of ovarian cancer2012/01/01English
Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts2012/01/01English
Use of unit standard paragraphs and letters in: 1. Australian Familial Cancer Centres 2. One Centre’s experience at Southern Health2012/01/01English
Clinical management of women in BRCAX families: issues and controversies2012/01/01English
Observation of the cancer patient journey: a learning curve for Genetic Counsellors2012/01/01English
Audit of adherence to GI screening recommendations for Lynch Syndrome Patients2012/01/01English
Whole genome sequencing in the study of disease and application in personalised medicine2012/01/01English
Identification of a novel disease-associated variant in the BRCA1 3’UTR that introduces a functional miR-103 target site2012/01/01English