The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome Susan StucklessPatrick S. ParfreyRoger C. Green Original Paper 13 October 2006 Pages: 1 - 12
The management of families affected by hereditary non-polyposis colorectal cancer (HNPCC) Johanne GearyHuw J. W. ThomasShirley V. Hodgson Original Paper 26 August 2006 Pages: 13 - 19
Molecular diagnosis of neurofibromatosis type 1: 2 years experience Siân GriffithsPeter ThompsonMeena Upadhyaya Original Paper 31 August 2006 Pages: 21 - 34
Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from Western Sweden Zakaria EinbeigiAnnika BergmanPer Karlsson ORIGINAL PAPER 31 August 2006 Pages: 35 - 41
The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family Marjo van PuijenbroekMaartje NielsenHans Morreau Original Paper 13 October 2006 Pages: 43 - 51
Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies R. C. GreenJ. S. GreenH. B. Younghusband Original Paper 13 October 2006 Pages: 53 - 62
Risks of cancer due to a single BRCA1 mutation in an extended Utah kindred Florian D. VoglMike D. BadziochDavid E. Goldgar Original Paper 19 October 2006 Pages: 63 - 71
Identification of a founder BRCA2 mutation in Sardinian breast cancer families Maria MonneGiovanna PirasAttilio Gabbas Original Paper 11 January 2007 Pages: 73 - 79
Familial colorectal cancer referral to regional genetics department—a single centre experience Tony MakDouglas SpeakeD. G. R. Evans Original paper 08 December 2006 Pages: 81 - 87
An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients Catherine F. LiRobert Y. WeiBenjamin A. Alman Original Paper 08 December 2006 Pages: 89 - 95
A missense germline mutation in exon 7 of the MSH2 gene in a HNPCC family from center-Italy Francesca BianchiEva GaliziaRiccardo Cellerino Original Paper 13 December 2006 Pages: 97 - 102
Study comparing two types of screening provision for people with von Hippel-Lindau disease Lindsay FraserSally WattsShirley Hodgson Original Paper 08 December 2006 Pages: 103 - 111
Improved survival in BRCA2 carriers with ovarian cancer Tuya PalJenny Permuth-WeyRebecca Sutphen Original Paper 08 December 2006 Pages: 113 - 119
The interval between cancer diagnosis among mothers and offspring in a population-based cohort Ora PaltielYehiel FriedlanderOrly Manor Original Paper 11 January 2007 Pages: 121 - 129
Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data D. A. van DijkM. J. OostindiërHereditary Tumor Study Group of the Comprehensive Cancer Centre West (CCCW) Original Paper Open access 20 January 2007 Pages: 131 - 134
Utility of computed tomographic colonography in surveillance for hereditary nonpolyposis colorectal cancer syndrome Laura Renkonen-SinisaloArto KivisaariHeikki J. Järvinen OriginalPaper 02 February 2007 Pages: 135 - 140
A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene M. VernezP. HutterH. Bouzourene Case Report 19 October 2006 Pages: 141 - 145
Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 gene W. StewartJ. P. TraynorE. S. Tobias Brief communication 31 August 2006 Pages: 147 - 152
Heterozygote BRCA1 status and skewed chromosome X inactivation Anne Helbling-LeclercGilbert M. LenoirJean Feunteun Short Communication 31 August 2006 Pages: 153 - 157
Acceptance of preventive surgeries by Israeli women who had undergone BRCA testing Vardit KramTamar PerezMichal Sagi Erratum 12 January 2007 Pages: 159 - 159
