Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer
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D. Hunter | P. Kraft | S. Hankinson | D. Cox
[1] H. Kazazian. Mobile Elements: Drivers of Genome Evolution , 2004, Science.
[2] Peter Donnelly,et al. A comparison of bayesian methods for haplotype reconstruction from population genotype data. , 2003, American journal of human genetics.
[3] Daniel O. Stram,et al. Modeling and E-M Estimation of Haplotype-Specific Relative Risks from Genotype Data for a Case-Control Study of Unrelated Individuals , 2003, Human Heredity.
[4] Paola Sebastiani,et al. Minimal haplotype tagging , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[5] J. Benítez,et al. Over-representation of two specific haplotypes among chromosomes harbouring BRCA1 mutations , 2003, European Journal of Human Genetics.
[6] J. Squire,et al. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors , 2002, Genes, chromosomes & cancer.
[7] B. Weber,et al. Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing. , 2000, American journal of human genetics.
[8] Simon Easteal,et al. Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees , 2000, Nature Genetics.
[9] D. Clayton,et al. Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population. , 1997, Human molecular genetics.
[10] J. Rossant,et al. The Tumor Suppressor Gene Brca1 Is Required for Embryonic Cellular Proliferation in the Mouse , 1996, Cell.
[11] M. Skolnick,et al. Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations. , 1996, Human molecular genetics.