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Familial 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 Currie
Familial Cancer|February 24, 2007
Two TP53 germline mutations in a classical Li-Fraumeni syndrome familyLiselotte P van Hest, Mariëlle W G Ruijs, Anja Wagner, et al.
Familial Cancer|April 7, 2007
Hysteroscopic findings in women at risk of HNPCC. Results of a prospective observational studyFabrice Lécuru, Ulrike Metzger, Catherine Scarabin, et al.
Familial Cancer|July 20, 2007
Germline mutations in the breast cancer susceptibility gene PTEN are rare in high-risk non-BRCA1/2 French Canadian breast cancer familiesFrédéric Guénard, Yvan Labrie, Geneviève Ouellette, et al.
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