| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion
|
Pho, Lana N.
|
|
2005
|
4 |
2 |
p. 135-138
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 5 |
APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers
|
Kariola, Reetta
|
|
2005
|
4 |
2 |
p. 187-190
|
article
|
| 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
|
article
|
| 7 |
High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia
|
Tikhomirova, Laima
|
|
2005
|
4 |
2 |
p. 77-84
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 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
|
article
|
| 12 |
Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers
|
Chenevix-Trench, G.
|
|
2005
|
4 |
2 |
p. 73-75
|
article
|
| 13 |
Referrals of patients to colorectal cancer genetics services in south-east Scotland
|
Holloway, Susan
|
|
2005
|
4 |
2 |
p. 151-161
|
article
|
| 14 |
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH
|
Akrami, Seyed Mohammad
|
|
2005
|
4 |
2 |
p. 145-149
|
article
|
| 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
|
article
|
| 16 |
The BRCA1 exon 13 duplication in the Swedish population
|
Kremeyer, Barbara
|
|
2005
|
4 |
2 |
p. 191-194
|
article
|
| 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
|
article
|
| 18 |
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds
|
Siddiqui, Rina
|
|
2005
|
4 |
2 |
p. 177-181
|
article
|
| 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
|
article
|
| 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
|
article
|
Journal description