Issue 1/2009
Content (12 Articles)
The 4154delA mutation carriers in the BRCA1 gene share a common ancestry
Silvija Ozolina, Olga Sinicka, Eriks Jankevics, Inna Inashkina, Jan Lubinski, Bohdan Gorski, Jacek Gronwald, Tatyana Nasedkina, Olga Fedorova, Ludmila Lyubchenko, Laima Tihomirova
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, Maggie Watson, Kathryn Kash, Robert Croyle, Rosalind Eeles
Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry
Bifeng Zhang, James D. Fackenthal, Qun Niu, Dezheng Huo, Walmy E. Sveen, Tiffani DeMarco, Clement A. Adebamowo, Temidayo Ogundiran, Olufunmilayo I. Olopade
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, K. Nathanson, S. M. Domchek
Absence of founder BRCA1 and BRCA2 mutations in coetaneous malignant melanoma patients of Ashkenazi origin
Luna Kadouri, Mark Temper, Tal Grenader, Dvorah Abeliovich, Tamar Hamburger, Tamar Peretz, Michal Lotem
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, Christopher J. Gostout
The FAP self-concept scale (adult form)
Mary Jane Esplen, Noreen Stuckless, Terri Berk, Kate Butler, Steve Gallinger
Identification 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, Kokichi Sugano, Hideyuki Ishida
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, Brenda L. Gallie, Dietmar R. Lohmann
Psychosocial impact of Peutz-Jeghers Syndrome
Alice Woo, Amit Sadana, David T. Mauger, Maria J. Baker, Terri Berk, Thomas J. McGarrity
MLPA mutation detection in Argentine HNPCC and FAP families
Laura C. Gomez, Diego M. Marzese, José Adi, Diego Bertani, Jorge Ibarra, Bart Mol, Ivonne Johanna Vos, Gabriela De Marchi, María Roqué
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, Torben F. Örntoft, Finn C. Nielsen, Lone Sunde, Anne-Marie Gerdes, Dorthe Cruger, Susanne Timshel, Marie-Louise Bisgaard, Inge Bernstein, Henrik Okkels