The 4154delA mutation carriers in the BRCA1 gene share a common ancestry Silvija OzolinaOlga SinickaLaima Tihomirova BriefCommunication 09 December 2008 Pages: 1 - 4
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 HallSusan GrayRosalind Eeles OriginalPaper 05 August 2008 Pages: 5 - 13
Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry Bifeng ZhangJames D. FackenthalOlufunmilayo I. Olopade OriginalPaper 05 August 2008 Pages: 15 - 22
Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomy C. A. GabrielJ. Tigges-CardwellS. M. Domchek OriginalPaper 29 August 2008 Pages: 23 - 28
Absence of founder BRCA1 and BRCA2 mutations in coetaneous malignant melanoma patients of Ashkenazi origin Luna KadouriMark TemperMichal Lotem OriginalPaper 05 August 2008 Pages: 29 - 32
Progression to advanced neoplasia is infrequent in post colectomy familial adenomatous polyposis patients under endoscopic surveillance Ferga C. GleesonGeorgios I. PapachristouChristopher J. Gostout OriginalPaper 23 July 2008 Pages: 33 - 38
The FAP self-concept scale (adult form) Mary Jane EsplenNoreen StucklessSteve Gallinger OriginalPaper 13 August 2008 Pages: 39 - 50
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 IwamaKouki KuwabaraHideyuki Ishida BriefCommunication Open access 15 August 2008 Pages: 51 - 54
Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma Diana MitterDiane RushlowDietmar R. Lohmann BriefCommunication 29 May 2008 Pages: 55 - 58
Psychosocial impact of Peutz-Jeghers Syndrome Alice WooAmit SadanaThomas J. McGarrity OriginalPaper 05 July 2008 Pages: 59 - 65
MLPA mutation detection in Argentine HNPCC and FAP families Laura C. GomezDiego M. MarzeseMaría Roqué OriginalPaper 10 July 2008 Pages: 67 - 73
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population Mef NilbertFriedrik P. WikmanHenrik Okkels OriginalPaper 20 June 2008 Pages: 75 - 83