The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies

The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studies

Mateus Pereira, Lutecia, H. (Laboratory of Population Genetics, National Cancer Institute)
Pineda, Marbin, A. (Laboratory of Population Genetics, National Cancer Institute)
Rowe, William, H. (Laboratory of Population Genetics, National Cancer Institute)
Fonseca, Liabia, R. (Department of Biological Sciences, Florida International University)
Greene, Mark, H. (Clinical Genetics Branch, National Cancer Institute)
Offit, Kenneth (Memorial Sloan Kettering Cancer Center)
Ellis, Nathan, A. (University of Chicago)
Zhang, Jinghui (Laboratory of Population Genetics, National Cancer Institute)
Collins, Andrew (Southampton General Hospital)
Struewing, Jeffery, P. (Laboratory of Population Genetics, National Cancer Institute)

2007-10-04

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2025-12-17

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DOI: https://doi.org/10.1186/1471-2156-8-68
fiu: FIDC003631

© 2007 Pereira et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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