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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion Pho, Lana N.
2005
4 2 p. 135-138
artikel
2 A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history Truta, Brindusa
2005
4 2 p. 127-133
artikel
3 A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques Bergman, Annika
2005
4 2 p. 89-96
artikel
4 An unusual case of Turcot’s syndrome associated with ileal adenocarcinoma, intestinal non-Hodgkin’s lymphoma, and duodenal adenocarcinoma. Review of the classification and genetic basis of Turcot’s syndrome Murphy, H. R.
2005
4 2 p. 139-143
artikel
5 APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers Kariola, Reetta
2005
4 2 p. 187-190
artikel
6 Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients Landsbergen, Karin
2005
4 2 p. 115-119
artikel
7 High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia Tikhomirova, Laima
2005
4 2 p. 77-84
artikel
8 Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study Mesters, Ilse
2005
4 2 p. 163-167
artikel
9 Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers Vadaparampil, Susan T.
2005
4 2 p. 195-206
artikel
10 Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort Phillips, Kelly-Anne
2005
4 2 p. 105-113
artikel
11 Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations Geirdal, Amy Østertun
2005
4 2 p. 121-126
artikel
12 Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers Chenevix-Trench, G.
2005
4 2 p. 73-75
artikel
13 Referrals of patients to colorectal cancer genetics services in south-east Scotland Holloway, Susan
2005
4 2 p. 151-161
artikel
14 Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH Akrami, Seyed Mohammad
2005
4 2 p. 145-149
artikel
15 SISE matters: the Sum of Information on Seventy-yr-old Equivalents measures pedigree information content when assessing the risk of HNPCC in a family Green, R. C.
2005
4 2 p. 169-175
artikel
16 The BRCA1 exon 13 duplication in the Swedish population Kremeyer, Barbara
2005
4 2 p. 191-194
artikel
17 The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families Sánchez de Abajo, Ana
2005
4 2 p. 183-186
artikel
18 The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds Siddiqui, Rina
2005
4 2 p. 177-181
artikel
19 The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews Quintana-Murci, Lluís
2005
4 2 p. 85-88
artikel
20 The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation Metcalfe, Kelly A.
2005
4 2 p. 97-103
artikel
                             20 gevonden resultaten
 
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