A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes

समान संसाधन

• Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2
  द्वारा: Goldgar, David E., और अन्य
  प्रकाशित: (2004)
• Functional Assays for Classification of BRCA2 Variants of Uncertain Significance
  द्वारा: Farrugia, Daniel J., और अन्य
  प्रकाशित: (2008)
• BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer
  द्वारा: Hall, Michael J., और अन्य
  प्रकाशित: (2009)
• A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data With Application to BRCA1
  द्वारा: Iversen, Edwin S., और अन्य
  प्रकाशित: (2011)
• An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)
  द्वारा: Chenevix-Trench, Georgia, और अन्य
  प्रकाशित: (2007)