Familial Cancer

BAP1 and Breast Cancer Risk

Isabelle Coupier, Pierre-Yves Cousin, David Hughes, Patricia Legoix-Né, Alexandra Trehin, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet

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, Carol J. Fabian

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, Fabio Aristizábal, Óscar Gutiérrez, Luis Alberto Ángel, Jorge Padrón, Carlos Martínez, Humberto Martínez, Omar Malaver, Luis Flórez, Rosa Barvo

Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like Families

Shiri Dovrat, Arie Figer, Herma H. Fidder, Pavlos Neophytou, Zvi Fireman, Ravit Geva, Jamal Zidan, Dov Flex, Shimon Bar Meir, Eitan Friedman

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, Juul Th. Wijnen, Hans F. A. Vasen, Conny A. van der Meer, Iris I. H. van Oostrom, Hanne Meijers-Heijboer

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, M.A. Nooij, G.G. Kenter, H.F.A. Vasen

Behavioral and Economic Impact of a Familial History of Cancers

Francois Eisinger, Carole Tarpin, Laetitia Huiart, Doug Horsman, Laetitia Rabayrol, Remi Didelot, Claire Julian-Reynier, Hagay Sobol

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, Jeffrey N. Weitzel

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, Eduardo Díaz-Rubio, Trinidad Caldés

Neurofibromatosis 2 (NF2) and Malignant Mesothelioma in a Man with a Constitutional NF2 Missense Mutation

M.E. Baser, H. Rai, A.J. Wallace, D.G.R. Evans

Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations

Prathap Bandipalliam

Acknowledgements

Key word Index Volume 4

Contents Volume 4