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August 1, 2002Journal of Medical GeneticsOpen Access

Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

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Authors

NKNoah D. KauffNorthwell HealthPPPedro Pérez‐SeguraHospital Clínico San Carlos
Mark E. Robson
Mark E. RobsonUniversity College Dublin

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Cite This Study

Kauff et al. (2002) studied this question.

synapsesocial.com/papers/6a6f934dfebe604dd7087814https://doi.org/10.1136/jmg.39.8.611
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Parity, Oral Contraceptives, and the Risk of Ovarian Cancer among Carriers and Noncarriers of a<i>BRCA1</i>or<i>BRCA2</i>Mutation2001 · 390 citations
  2. 2Probability of Carrying a Mutation of Breast-Ovarian Cancer Gene BRCA1 Based on Family History1997 · 382 citations
  3. 3Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families1998 · 3,051 citations
  4. 4Genetic Susceptibility and Survival: Application to Breast Cancer2000 · 8 citations