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

N. D. Kauff, P. Perez-Segura, M. E. Robson, L. Scheuer, B. Siegel, A. Schluger, B. Rapaport, T. S. Frank, K. Nafa, N. A. Ellis, G. Parmigiani, K. Offit

Research output: Contribution to journalArticle

83 Scopus citations
Original languageEnglish (US)
Pages (from-to)611-614
Number of pages4
JournalJournal of Medical Genetics
Volume39
Issue number8
DOIs
StatePublished - 2002

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Kauff, N. D., Perez-Segura, P., Robson, M. E., Scheuer, L., Siegel, B., Schluger, A., Rapaport, B., Frank, T. S., Nafa, K., Ellis, N. A., Parmigiani, G., & Offit, K. (2002). Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families. Journal of Medical Genetics, 39(8), 611-614. https://doi.org/10.1136/jmg.39.8.611