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Familial Cancer|July 22, 2006
Family history, and impact on clinical presentation and prognosis, in a population-based breast cancer cohort from the Stockholm CountySara Margolin, Hemming Johansson, Lars Erik Rutqvist, et al.Familial Cancer|July 11, 2006
BRCA1 and BRCA2 germline mutational spectrum and evidence for genetic anticipation in Portuguese breast/ovarian cancer familiesAna Peixoto, Natália Salgueiro, Catarina Santos, et al.Familial Cancer|June 1, 2006
BRCA1 and BRCA2: chemosensitivity, treatment outcomes and prognosisWilliam D FoulkesFamilial Cancer|June 1, 2006
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patientsM Spaepen, B Vankeirsbilck, S Van Opstal, et al.Familial Cancer|June 1, 2006
Desmoid tumors -- a characterization of patients seen at Mayo Clinic 1976-1999Taya Fallen, Marcia Wilson, Bruce Morlan, et al.Familial Cancer|June 1, 2006
The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype with incomplete penetrance: implications for screening and management of carrier statusTabib Dabir, Steven J Hunter, Colin F J Russell, et al.Familial Cancer|May 18, 2007
Delivery of cancer genetics services: The Royal Marsden telephone clinic modelS Shanley, K Myhill, R Doherty, et al.Familial Cancer|May 24, 2007
Patient perspectives on the Poole PCT cancer genetics serviceHelen Allen, Lynn Maxwell, Nikki Dibley, et al.Familial Cancer|May 24, 2007
Improving access to cancer genetics services in primary care: socio-economic data from North KirkleesJ Srinivasa, E Rowett, N Dharni, et al.Familial Cancer|May 24, 2007
National evaluation of NHS genetics service investments: emerging issues from the cancer genetics pilotsGraham P Martin, Rachael Finn, Graeme CurriePageof 152