10 rare tumors that warrant a genetics referral Kimberly C. BanksJessica J. MolineKristen J. Vogel Review 28 November 2012 Pages: 1 - 18
Catalysts to withdrawal from familial ovarian cancer screening for surgery and reactions to discontinued screening: a qualitative study Kate J. LiffordAlison ClementsKate Brain Original Article 27 September 2012 Pages: 19 - 26
Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors Isabelle SourrouilleFlorence CouletFlorent Soubrier Original Article 18 September 2012 Pages: 27 - 33
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families Lucie SchwarzováJitka ŠtekrováMilada Kohoutová Original Article 18 September 2012 Pages: 35 - 42
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review A. P. KnoppertsM. NielsenF. J. Hes Original Article 25 September 2012 Pages: 43 - 50
Prospective enteroscopic evaluation of jejunal polyposis in patients with familial adenomatous polyposis and advanced duodenal polyposis Y. A. AlderliesteE. A. J. RauwsE. Dekker Original Article 29 September 2012 Pages: 51 - 56
The spectrum of urological malignancy in Lynch syndrome P. J. BarrowS. InghamD. G. Evans Original Article 11 October 2012 Pages: 57 - 63
Feasibility evaluation of an online tool to guide decisions for BRCA1/2 mutation carriers Elizabeth A. SchackmannDiego F. MunozAllison W. Kurian Original Article 21 October 2012 Pages: 65 - 73
The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study Sang-Ah HanSung-Won KimThe KOHBRA Research Group and the Korean Breast Cancer Society Original Article 07 November 2012 Pages: 75 - 81
An unusual BRCA mutation distribution in a high risk cancer genetics clinic Anna C. Nelson-MosekeJoanne M. JeterChristina M. Laukaitis Original Article 21 November 2012 Pages: 83 - 87
Multiple small “imaging” branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia? D. K. BartschK. DietzelP. Langer Original Article 22 November 2012 Pages: 89 - 96
Birt–Hogg–Dubé: beyond the clinical manifestations Lindsay A. Middelton Original Article 23 November 2012 Pages: 97 - 99
Psychosocial factors and uptake of risk-reducing salpingo-oophorectomy in women at high risk for ovarian cancer Bettina MeiserMelanie A. PriceKelly-Anne Phillips Original Article 01 December 2012 Pages: 101 - 109
A novel missense mutation (N78D) in a family with von Hippel–Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts S. CingozR. B. van der LuijtMihriban Heval Ozgen Original Article 09 December 2012 Pages: 111 - 117
The deletion of exons 3–5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families Sarai PalancaInmaculada de JuanPascual Bolufer Short Communication 02 November 2012 Pages: 119 - 123
Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier Shaheen AlaneeSohela ShahKenneth Offit Letter to the Editor 20 October 2012 Pages: 125 - 127
Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation Ekatherina Sh. KuliginaAnna P. SokolenkoEvgeny N. Imyanitov Letter to the Editor 27 October 2012 Pages: 129 - 132
The Fourth Birt–Hogg–Dubé Symposium, Cincinnati, USA, 28th–30th March, 2012 Abstracts 03 July 2012 Pages: 133 - 140