BAP1 and Breast Cancer Risk Isabelle CoupierPierre-Yves CousinDominique Stoppa-Lyonnet OriginalPaper Pages: 273 - 277
Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial Jennifer R. KlempAnne O’DeaCarol J. Fabian OriginalPaper Pages: 279 - 284
MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations Alejandro GiraldoAndrea GómezRosa Barvo OriginalPaper Pages: 285 - 290
Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families Shiri DovratArie FigerEitan Friedman OriginalPaper Pages: 291 - 294
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures Anja WagnerIngrid van KesselHanne Meijers-Heijboer OriginalPaper Pages: 295 - 300
Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect Th.E.M. CrijnenM.L.G. Janssen-HeijnenH.F.A. Vasen OriginalPaper Pages: 301 - 305
Behavioral and Economic Impact of a Familial History of Cancers Francois EisingerCarole TarpinHagay Sobol OriginalPaper Pages: 307 - 311
Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability Sharon R. SandDavid S. DeRamJeffrey N. Weitzel Short communication Pages: 313 - 316
Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families Miguel de la HoyaJuan Manuel FernándezTrinidad Caldés Short communication Pages: 317 - 319
Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation M.E. BaserH. RaiD.G.R. Evans Case report Pages: 321 - 322
Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations Prathap Bandipalliam Review Pages: 323 - 333
