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November 9, 2020Open Access

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

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A 2020 study studied this question.

synapsesocial.com/papers/6a887c3a2c11edba2ecf2c49https://doi.org/10.17615/jkkh-v976
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Also Consider

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  1. 1Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.1996 · 340 citations
  2. 2Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q211990 · 2,564 citations