Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases – preliminary report

This publication has 34 references indexed in Scilit:

• Understanding missense mutations in the BRCA1 gene: An evolutionary approach
  Proceedings of the National Academy of Sciences, 2003
• Structural Consequences of a Cancer-causing BRCA1-BRCT Missense Mutation
  Journal of Biological Chemistry, 2003
• BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping
  American Journal of Human Genetics, 2002
• The R71GBRCA1is a founder Spanish mutation and leads to aberrant splicing of the transcript
  Human Mutation, 2001
• A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
  Nature Genetics, 2001
• Mutation in the coding region of theBRCA1 gene leads to aberrant splicing of the transcript
  Human Mutation, 1999
• A BRCA1 Nonsense Mutation Causes Exon Skipping
  American Journal of Human Genetics, 1998
• Mutations and alternative splicing of theBRCA1 gene in UK breast/ovarian cancer families
  Genes, Chromosomes and Cancer, 1997
• The genetic attributable risk of breast and ovarian cancer
  Cancer, 1996
• Genetic risk and screening techniques for epithelial ovarian cancer
  International Journal of Gynecology & Obstetrics, 1993