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Volume 1 / 2001 - Volume 10 / 2011
1-7
An audit of familial juvenile polyposis at the Tel Aviv Medical Center: demographic, genetic and clinical features
Paul Rozen, Ziona Samuel, Eli Brazowski, Markus Jakubowicz and Jacob Rattan, et al.
9-13
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours
Astrid T. Stormorken, Wolfram Müller, Annika Lindblom, Ketil Heimdal and Steinar Aase, et al.
15-25
Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility?
Sara Levene, Gillian Scott, Patricia Price, Jeremy Sanderson and Helen Evans, et al.
27-33
Quality of life in patients with multiple endocrine neoplasia type 1 (MEN1)
G. Berglund, A. Lidén, M. G. Hansson, K. Öberg and P. O. Sjöden, et al.
35-42
The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testing
Alexandre Sibert and David E. Goldgar
43-55
Attenuated familial adenomatous polyposis (AFAP): a review of the literature
Anne Lyster Knudsen, Marie Luise Bisgaard and Steffen Bülow
57-67
Genetic susceptibility to prostate cancer: a review
Bas A. J. Verhage and Lambertus A. L. M. Kiemeney
69-71
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