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                             21 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An audit of familial juvenile polyposis at the Tel Aviv Medical Center: demographic, genetic and clinical features Rozen, Paul
2003
2 1 p. 1-7
artikel
2 An audit of familial juvenile polyposis at the Tel Aviv Medical Center: demographic, genetic and clinical features Paul Rozen
2003
2 1 p. 1-7
8 p.
artikel
3 Attenuated familial adenomatous polyposis (AFAP): a review of the literature Knudsen, Anne Lyster
2003
2 1 p. 43-55
artikel
4 Attenuated familial adenomatous polyposis (AFAP): a review of the literature Anne Lyster Knudsen
2003
2 1 p. 43-55
13 p.
artikel
5 Author index 2003
2 1 p. 91-95
artikel
6 Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility? Levene, Sara
2003
2 1 p. 15-25
artikel
7 Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility? Sara Levene
2003
2 1 p. 15-25
11 p.
artikel
8 Free Paper 2003
2 1 p. 19-90
artikel
9 Genetic susceptibility to prostate cancer: a review Verhage, Bas A. J.
2003
2 1 p. 57-67
artikel
10 Genetic susceptibility to prostate cancer: a review Bas A. J. Verhage
2003
2 1 p. 57-67
11 p.
artikel
11 History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer Lynch, Henry T.
2003
2 1 p. 3-5
artikel
12 Instructions for authors 2003
2 1 p. 69-71
artikel
13 Instructions for authors 2003
2 1 p. 69-71
3 p.
artikel
14 Origins of the Leeds Castle Polyposis Group Neale, Kay
2003
2 1 p. 1-2
artikel
15 Program 2003
2 1 p. 7-17
artikel
16 Quality of life in patients with multiple endocrine neoplasia type 1 (MEN1) Berglund, G.
2003
2 1 p. 27-33
artikel
17 Quality of life in patients with multiple endocrine neoplasia type 1 (MEN 1) G. Berglund
2003
2 1 p. 27-33
7 p.
artikel
18 The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testing Sibert, Alexandre
2003
2 1 p. 35-42
artikel
19 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
2003
2 1 p. 35-42
8 p.
artikel
20 The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours Stormorken, Astrid T.
2003
2 1 p. 9-13
artikel
21 The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours Astrid T. Stormorken
2003
2 1 p. 9-13
5 p.
artikel
                             21 gevonden resultaten
 
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