The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia Zhi L. TeoSarah D. SawyerMelissa C. Southey Letter to the Editor 08 March 2013 Pages: 587 - 595
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer Shaheen AlaneeSohela ShahKenneth Offit Original Article 09 March 2013 Pages: 597 - 600
Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends? Julie LapointeMichel DorvalClaire Julian-Reynier Original Article 09 March 2013 Pages: 601 - 610
Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome Katsunori FujiiHirofumi OhashiToshiyuki Miyashita Original Article 12 March 2013 Pages: 611 - 614
Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers Tuya PalSusan VadaparampilKelly Metcalfe Original Article 16 March 2013 Pages: 615 - 619
Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation Dongwon KimEunyoung KangSung-Won Kim Original Article 16 March 2013 Pages: 621 - 628
Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer? Karen BronnerIlse MestersRevital Kariv Original Article 02 April 2013 Pages: 629 - 637
Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study Katja Aktan-CollanHelena KääriäinenAri Haukkala Original Article 20 March 2013 Pages: 639 - 646
Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient G. I. Butel-SimoesA. D. Spigelman Original Article 21 April 2013 Pages: 647 - 649
Self administered screening for hereditary cancers in conjunction with mammography and ultrasound Charles H. McDonnellDavid J. SeidenwurmKristie A. Bobolis Original Article 13 April 2013 Pages: 651 - 656
Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia Jie ZhuLiang CuiJiang-Ping Gao Original Article 11 June 2013 Pages: 657 - 667
Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives Yark HazewinkelJohannes B. ReitsmaEvelien Dekker Original Article 17 April 2013 Pages: 669 - 673
Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes Aisha S. SieJudith B. PrinsNicoline Hoogerbrugge Original Article 21 April 2013 Pages: 675 - 682
Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients Grigorijs PlakhinsArvids IrmejsJanis Gardovskis Original Article 03 May 2013 Pages: 683 - 689
Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer Beata BielinskaPawel GajJanusz A. Siedlecki Original Article 09 May 2013 Pages: 691 - 698
“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis” Yasser A. AlderliesteBarbara A. BastiaansenEvelien Dekker Original Article 10 May 2013 Pages: 699 - 706
Chemoprevention in Lynch syndrome John BurnJohn C. MathersD. Tim Bishop Original Paper 24 July 2013 Pages: 707 - 718
Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry Murray Joseph CaseyChhanda BewtraPatrice Watson Original Article 12 May 2013 Pages: 719 - 740
Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity M. P. FarrellD. J. HughesD. J. Gallagher Original Article 28 May 2013 Pages: 741 - 747
Rectal cancers in patients with familial adenomatous polyposis Jennifer LiangJames M. Church Original Article 16 May 2013 Pages: 749 - 754
Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer Shuying LiXiaojuan ZhaoYashuang Zhao Original Article 29 May 2013 Pages: 755 - 765
Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence Inmaculada de Juan JiménezZaida García CasadoPascual Bolufer Gilabert Short Communication 12 March 2013 Pages: 767 - 777
The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012 Abstracts 01 May 2013 Pages: 779 - 809
