Hereditary medullary thyroid carcinoma: the management dilemma Ping ZhouJian LiuLing Peng Review 20 December 2011 Pages: 157 - 165
Management of duodenal adenomatosis in FAP: single centre experience Musa DriniAnthony SpeerFinlay A. Macrae Original Article 01 December 2011 Pages: 167 - 173
Preimplantation genetic diagnosis for inherited breast cancer: first clinical application and live birth in Spain Teresa Ramón y CajalAna PoloJoaquin Calaf Original Article 18 December 2011 Pages: 175 - 179
Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families S. M. SchneegansA. RosenbergerM. Shoukier Original Article Open access 13 December 2011 Pages: 181 - 188
A novel germline SDHB mutation in a gastrointestinal stromal tumor patient without bona fide features of the Carney–Stratakis dyad Ricardo CelestinoJorge LimaJosé Manuel Lopes Original Article 10 December 2011 Pages: 189 - 194
Urologists’ and GPs’ knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands Ruben CremersChristi van AsperenLambertus Kiemeney Original Article Open access 11 December 2011 Pages: 195 - 200
Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening Angela M. CozzolinoLucia PedacePaola Grammatico Original Article 25 December 2011 Pages: 201 - 208
Active surveillance of renal masses in von Hippel-Lindau disease: growth rates and clinical outcome over a median follow-up period of 56 months Jin ZhangJia-Hua PanYi-Ran Huang Original Article 28 December 2011 Pages: 209 - 214
Looking different, feeling different: women’s reactions to risk-reducing breast and ovarian surgery Nina HallowellBrandi BaylockMelanie A. Price Original Article 24 December 2011 Pages: 215 - 224
RB1 mutations and second primary malignancies after hereditary retinoblastoma Charlotte J. DommeringTamara MareesAnnette C. Moll Original Article Open access 29 December 2011 Pages: 225 - 233
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations A. MoranC. O’HaraD. G. R. Evans Original Article 21 December 2011 Pages: 235 - 242
The founder Ashkenazi Jewish mutations in the MSH2 and MSH6 genes in Israeli patients with gastric and pancreatic cancer Yael LaitmanLiron HerskovitzEitan Friedman Original Article 04 January 2012 Pages: 243 - 247
Can a gastrointestinal pathologist identify microsatellite instability in colorectal cancer with reproducibility and a high degree of specificity? Eli BrazowskiPaul RozenGuy Rosner Original Article 13 January 2012 Pages: 249 - 257
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist’s initiative K. M. LandsbergenJ. B. PrinsN. Hoogerbrugge Original Article Open access 07 February 2012 Pages: 259 - 267
French women’s breast self-examination practices with time after undergoing BRCA1/2 genetic testing C. MaheuT. ApostolidisC. Julian-Reynier Original Article 18 February 2012 Pages: 269 - 278
Predictive genetic testing of first degree relatives of mutation carriers is a cost-effective strategy in preventing hereditary non-polyposis colorectal cancer in Singapore Vivian Wei WangPoh Koon KohJeremy Fung Yen Lim Original Article 17 February 2012 Pages: 279 - 289
Families’ experience of oncogenetic counselling: accounts from a heterogeneous hereditary cancer risk population Álvaro MendesLiliana Sousa Original Article 25 February 2012 Pages: 291 - 306
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients Muhammad U. RashidSidra GullUte Hamann Short Communication 07 February 2012 Pages: 307 - 311
