273-277
BAP1 and Breast Cancer Risk
Isabelle Coupier, Pierre-Yves Cousin, David Hughes, Patricia Legoix-Né and Alexandra Trehin, et al.
279-284
Patient Satisfaction of BRCA1/2 Genetic Testing by Women at High Risk for Breast Cancer Participating in a Prevention Trial
Jennifer R. Klemp, Anne O’Dea, Carolyn Chamberlain and Carol J. Fabian
285-290
MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations
Alejandro Giraldo, Andrea Gómez, Gustavo Salguero, Herbert García and Fabio Aristizábal, et al.
291-294
Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families
Shiri Dovrat, Arie Figer, Herma H. Fidder, Pavlos Neophytou and Zvi Fireman, et al.
295-300
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures
Anja Wagner, Ingrid van Kessel, Mieke G. Kriege, Carli M. J. Tops and Juul Th. Wijnen, et al.
301-305
Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect
Th.E.M. Crijnen, M.L.G. Janssen-Heijnen, H. Gelderblom, J. Morreau and M.A. Nooij, et al.
307-311
Behavioral and Economic Impact of a Familial History of Cancers
Francois Eisinger, Carole Tarpin, Laetitia Huiart, Doug Horsman and Laetitia Rabayrol, et al.
313-316
Short communication
Linkage of a Pedigree Drawing Program and Database to a Program for Determining BRCA Mutation Carrier Probability
Sharon R. Sand, David S. DeRam, Deborah J. MacDonald, Kathleen R. Blazer and Jeffrey N. Weitzel
317-319
Short communication
Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families
Miguel de la Hoya, Juan Manuel Fernández, Ana Sánchez de Abajo, Alicia Tosar and Eduardo Díaz-Rubio, et al.
321-322
Case report
Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation
M.E. Baser, H. Rai, A.J. Wallace and D.G.R. Evans
323-333
Review
Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations
Prathap Bandipalliam
335
Acknowledgements
337-338
Key word Index Volume 4
339-342
Contents Volume 4