A deletion/insertion mutation in theBRCA2 gene in a breast cancer family: A possible role of theAlu-polyA tail in the evolution of the deletion
- 22 February 2001
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 31 (1), 91-95
- https://doi.org/10.1002/gcc.1110
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- AnAlu-mediated 7.1 kb deletion ofBRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10Genes, Chromosomes and Cancer, 2000
- Exon Deletions and Duplications in BRCA1 Detected by Semiquantitative PCRGenetic Testing, 2000
- Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer familiesOncogene, 1999
- Alu Repeats and Human DiseaseMolecular Genetics and Metabolism, 1999
- A complete protein truncation test for BRCA1 and BRCA2European Journal of Human Genetics, 1998
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer FamiliesAmerican Journal of Human Genetics, 1998
- Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocolsEuropean Journal of Human Genetics, 1998
- BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patientsNature Genetics, 1997
- Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer familyHuman Molecular Genetics, 1997
- Mutation analysis in the BRCA2 gene in primary breast cancersNature Genetics, 1996