1-4
The 4154delA mutation carriers in the BRCA1 gene share a common ancestry
Silvija Ozolina, Olga Sinicka, Eriks Jankevics, Inna Inashkina and Jan Lubinski, et al.
5-13
Genetic testing for BRCA1: effects of a randomised study of knowledge provision on interest in testing and long term test uptake; implications for the NICE guidelines
Julia Hall, Susan Gray, Roger A’Hern, Susan Shanley and Maggie Watson, et al.
15-22
Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry
Bifeng Zhang, James D. Fackenthal, Qun Niu, Dezheng Huo and Walmy E. Sveen, et al.
23-28
Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomy
C. A. Gabriel, J. Tigges-Cardwell, J. Stopfer, J. Erlichman and K. Nathanson, et al.
29-32
Absence of founder BRCA1 and BRCA2 mutations in coetaneous malignant melanoma patients of Ashkenazi origin
Luna Kadouri, Mark Temper, Tal Grenader, Dvorah Abeliovich and Tamar Hamburger, et al.
33-38
Progression to advanced neoplasia is infrequent in post colectomy familial adenomatous polyposis patients under endoscopic surveillance
Ferga C. Gleeson, Georgios I. Papachristou, Douglas L. Riegert-Johnson, Anne-Marie Boller and Christopher J. Gostout
39-50
The FAP self-concept scale (adult form)
Mary Jane Esplen, Noreen Stuckless, Terri Berk, Kate Butler and Steve Gallinger
51-54
Open AccessIdentification of somatic APC mutations in recurrent desmoid tumors in a patient with familial adenomatous polyposis to determine actual recurrence of the original tumor or de novo occurrence
Takeo Iwama, Kouki Kuwabara, Mineko Ushiama, Teruhiko Yoshida and Kokichi Sugano, et al.
55-58
Identification of a mutation in exon 27 of the
RB1
gene associated with incomplete penetrance retinoblastoma
Diana Mitter, Diane Rushlow, Inga Nowak, Birgit Ansperger-Rescher and Brenda L. Gallie, et al.
59-65
Psychosocial impact of Peutz-Jeghers Syndrome
Alice Woo, Amit Sadana, David T. Mauger, Maria J. Baker and Terri Berk, et al.
67-73
MLPA mutation detection in Argentine HNPCC and FAP families
Laura C. Gomez, Diego M. Marzese, José Adi, Diego Bertani and Jorge Ibarra, et al.
75-83
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population
Mef Nilbert, Friedrik P. Wikman, Thomas V. O. Hansen, Henrik B. Krarup and Torben F. Örntoft, et al.