1. Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review

   • Alexander M. Metcalf
   • Amanda B. Spurdle

   Review 24 July 2013 Pages: 1 - 12

   

2. Mammographic surveillance in women aged 35–39 at enhanced familial risk of breast cancer (FH02)

   • D. G. Evans
   • S. Thomas
   • S. Duffy

   Original Article 04 June 2013 Pages: 13 - 21

3. The prevalence of small intestinal polyps in patients with familial adenomatous polyposis: a prospective capsule endoscopy study

   • Atsuo Yamada
   • Hirotsugu Watabe
   • Kazuhiko Koike

   Original Article 07 June 2013 Pages: 23 - 28

   

4. No evidence of genetic anticipation in a large family with Lynch syndrome

   • D. Stupart
   • P. Goldberg
   • R. Ramesar

   Original Article 16 June 2013 Pages: 29 - 34

   

5. Does and should breast cancer genetic counselling include lifestyle advice?

   • Akke Albada
   • Madelèn Vernooij
   • Margreet G. E. M. Ausems

   Original Article 11 August 2013 Pages: 35 - 44

6. Genetic variation at 8q24, family history of cancer, and upper gastrointestinal cancers in a Chinese population

   • Heather P. Tarleton
   • Shen-Chih Chang
   • Zuo-Feng Zhang

   Original Article 13 September 2013 Pages: 45 - 56

7. Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome

   • Marry H. Nieuwenhuis
   • C. Marleen Kets
   • Hans F. A. Vasen

   Original Article 11 August 2013 Pages: 57 - 63

   

8. Lynch Syndrome in high risk Ashkenazi Jews in Israel

   • Yael Goldberg
   • Inbal Kedar
   • Tamar Peretz

   Original Article 30 August 2013 Pages: 65 - 73

   

9. Reflex testing for Lynch syndrome: If we build it, will they come? Lessons learned from the uptake of clinical genetics services by individuals with newly diagnosed colorectal cancer (CRC)

   • E. Tomiak
   • A. Samson
   • T. Asmis

   Original Article Open access 04 September 2013 Pages: 75 - 82

10. Illness perceptions, risk perception and worry in SDH mutation carriers

    • L. T. van Hulsteijn
    • A. A. Kaptein
    • E. P. M. Corssmit

    Original Article 30 August 2013 Pages: 83 - 91

11. Lack of association between let-7 binding site polymorphism rs712 and risk of nasopharyngeal carcinoma

    • Xin-Min Pan
    • Jing Jia
    • Lin-Bo Gao

    Original Article 31 August 2013 Pages: 93 - 97

12. Impact of breast cancer family history on tumor detection and tumor size in women newly-diagnosed with invasive breast cancer

    • Fabienne Dominique Schwab
    • Nicole Bürki
    • Uwe Güth

    Original Article 04 September 2013 Pages: 99 - 107

13. Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer

    • Pilar Garre
    • Lorena Martín
    • Trinidad Caldés

    Original Article 06 September 2013 Pages: 109 - 119

    

14. MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours

    • Joakim Crona
    • Rajani Maharjan
    • Peyman Björklund

    Short Communication 07 June 2013 Pages: 121 - 125

15. The MDM2 285G–309G haplotype is associated with an earlier age of tumour onset in patients with Li-Fraumeni syndrome

    • Mariette Renaux-Petel
    • Richard Sesboüé
    • Gaëlle Bougeard

    Short Communication 25 July 2013 Pages: 127 - 130

16. Diversity of the clinical presentation of the MMR gene biallelic mutations

    • Gaëlle Bougeard
    • Laurence Olivier-Faivre
    • Thierry Frebourg

    Short Communication 26 September 2013 Pages: 131 - 135