Some public health issues in the current state of genetic testing for breast cancer in Australia
Open Access
- 1 October 1996
- journal article
- review article
- Published by Elsevier in Australian and New Zealand Journal of Public Health
- Vol. 20 (5), 467-472
- https://doi.org/10.1111/j.1467-842x.1996.tb01623.x
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Risk Factors for Breast Cancer According to Family History of Breast CancerJNCI Journal of the National Cancer Institute, 1996
- Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlationNature Genetics, 1995
- Identification of the breast cancer susceptibility gene BRCA2Nature, 1995
- The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsNature Genetics, 1995
- Familial Clustering of Breast and Prostate Cancers and Risk of Postmenopausal Breast CancerJNCI Journal of the National Cancer Institute, 1994
- Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer ProbandsJNCI Journal of the National Cancer Institute, 1994
- Breast Cancer Risks in Relatives of Male Breast Cancer PatientsJNCI Journal of the National Cancer Institute, 1992
- Projecting Individualized Probabilities of Developing Breast Cancer for White Females Who Are Being Examined AnnuallyJNCI Journal of the National Cancer Institute, 1989
- Breast and Other Cancers in Families with Ataxia-TelangiectasiaNew England Journal of Medicine, 1987
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971