Testing for BRCA1 mutations: a cost-effectiveness analysis
- 2 October 2002
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 10 (10) , 599-606
- https://doi.org/10.1038/sj.ejhg.5200854
Abstract
The European Journal of Human Genetics is the official Journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports, News and Commentary articles and reviews in the rapidly expanding field of human genetics and genomics.Keywords
This publication has 35 references indexed in Scilit:
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer FamiliesAmerican Journal of Human Genetics, 1998
- BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patientsNature Genetics, 1997
- The Risk of Cancer Associated with Specific Mutations ofBRCA1andBRCA2among Ashkenazi JewsNew England Journal of Medicine, 1997
- The genetic epidemiology of BRCA1The Lancet, 1994
- Efficient detection of point mutations on color-codedstrands of target DNA.Proceedings of the National Academy of Sciences, 1994
- Risks of cancer in BRCA1-mutation carriersThe Lancet, 1994
- Detecting single base substitutions as heteroduplex polymorphismsGenomics, 1992
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989
- Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.Proceedings of the National Academy of Sciences, 1989
- DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory.Proceedings of the National Academy of Sciences, 1983