An audit of familial juvenile polyposis at the Tel Aviv Medical Center: demographic, genetic and clinical features Paul RozenZiona SamuelZamir Halpern OriginalPaper Pages: 1 - 7
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours Astrid T. StormorkenWolfram MüllerPål Møller OriginalPaper Pages: 9 - 13
Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility? Sara LeveneGillian ScottShirley Hodgson OriginalPaper Pages: 15 - 25
Quality of life in patients with multiple endocrine neoplasia type 1 (MEN1) G. BerglundA. LidénK. Nordin OriginalPaper Pages: 27 - 33
The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testing Alexandre SibertDavid E. Goldgar OriginalPaper Pages: 35 - 42
Attenuated familial adenomatous polyposis (AFAP): a review of the literature Anne Lyster KnudsenMarie Luise BisgaardSteffen Bülow ReviewPaper Pages: 43 - 55
Genetic susceptibility to prostate cancer: a review Bas A. J. VerhageLambertus A. L. M. Kiemeney ReviewPaper Pages: 57 - 67