Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers G. Chenevix-TrenchO. M. SinilnikovakConFab OriginalPaper Pages: 73 - 75
High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia Laima TikhomirovaOlga SinickaAivars Stengrevics OriginalPaper Pages: 77 - 84
The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi Jews Lluís Quintana-MurciInbar GalEitan Friedman OriginalPaper Pages: 85 - 88
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques Annika BergmanAnna FlodinMargareta Nordling OriginalPaper Pages: 89 - 96
The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation Kelly A. MetcalfeCarrie SnyderSteven Narod OriginalPaper Pages: 97 - 103
Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort Kelly-Anne PhillipsPhyllis N. ButowJohn L. Hopper OriginalPaper Pages: 105 - 113
Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients Karin LandsbergenChris VerhaakNicoline Hoogerbrugge OriginalPaper Pages: 115 - 119
Psychological distress in women at risk of hereditary breast/ovarian or HNPCC cancers in the absence of demonstrated mutations Amy Østertun GeirdalJon G. ReicheltPål Møller OriginalPaper Pages: 121 - 126
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history Brindusa TrutaBrian A. AllenJonathan P. Terdiman OriginalPaper Pages: 127 - 133
Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion Lana N. PhoCheryl M. CoffinRandall W. Burt OriginalPaper Pages: 135 - 138
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 H. R. MurphyW. TaylorR. Sturgess OriginalPaper Pages: 139 - 143
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH Seyed Mohammad AkramiMalcolm G. DunlopJohn A. L. Armour OriginalPaper Pages: 145 - 149
Referrals of patients to colorectal cancer genetics services in south-east Scotland Susan HollowayMary PorteousHarry Campbell OriginalPaper Pages: 151 - 161
Informing one’s family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study Ilse MestersMarlein AusemsHans Vasen OriginalPaper Pages: 163 - 167
SISE matters: the Sum of Information on Seventy-yr-old Equivalents measures pedigree information content when assessing the risk of HNPCC in a family R. C. GreenJ. R. McLaughlinH. B. Younghusband OriginalPaper Pages: 169 - 175
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li–Fraumeni-like kindreds Rina SiddiquiKenan OnelKenneth Offit OriginalPaper Pages: 177 - 181
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families Ana Sánchez de AbajoMiguel de la HoyaTrinidad Caldés OriginalPaper Pages: 183 - 186
APC and β-catenin protein expression patterns in HNPCC-related endometrial and colorectal cancers Reetta KariolaWael M. Abdel-RahmanMinna Nyström OriginalPaper Pages: 187 - 190
The BRCA1 exon 13 duplication in the Swedish population Barbara KremeyerMaria SollerAnnika Lindblom Letter to the editor Pages: 191 - 194
Measurement of psychological factors associated with genetic testing for hereditary breast, ovarian and colon cancers Susan T. VadaparampilMary RopkaMichael E. Stefanek Review Pages: 195 - 206