Ausgabe 1/2016
Inhalt (18 Artikel)
The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes
Nabil Amara, Jolyane Blouin-Bougie, Jalila Jbilou, Norrin Halilem, Jacques Simard, Réjean Landry
Screening of HELQ in breast and ovarian cancer families
Liisa M. Pelttari, Laura Kinnunen, Johanna I. Kiiski, Sofia Khan, Carl Blomqvist, Kristiina Aittomäki, Heli Nevanlinna
Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned
Bich-Thu Duong, Ravi Savarirayan, Ingrid Winship
Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients
Daniel Robert Quast, Ralph Schneider, Emanuel Burdzik, Steffen Hoppe, Gabriela Möslein
Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer?
Bar Chikman, Tima Davidson, Hasan Kais, Igor Jeroukhimov, Ari Leshno, Judith Sandbank, Ariel Halevy, Ron Lavy
Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects
Camelia Abdel-Malak, Hossam Darwish, Afaf Elsaid, Fatma El-Tarapely, Rami Elshazli
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz–Jeghers syndrome
Victoria McKay, Diane Cairns, David Gokhale, Roger Mountford, Lynn Greenhalgh
Genetic testing for Lynch syndrome: family communication and motivation
Celine H. M. Leenen, Mariska den Heijer, Conny van der Meer, Ernst J. Kuipers, Monique E. van Leerdam, Anja Wagner
Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study
Minori Matsumoto, Takeshi Nakajima, Yasuo Kakugawa, Taku Sakamoto, Shiko Kuribayashi, Yosuke Otake, Takahisa Matsuda, Yukihide Kanemitsu, Hirokazu Taniguchi, Yutaka Saito
Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary
Janos Papp, Marietta Eva Kovacs, Zoltan Matrai, Enikő Orosz, Miklós Kásler, Anne-Lise Børresen-Dale, Edith Olah
Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives
Junyi Wang, Bin Zhang, Wensheng Liu, Yongxia Zhang, Xuebing Di, Yanmei Yang, Dangui Yan
Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry
Kris Ann P. Schultz, Anne Harris, Yoav Messinger, Susan Sencer, Shari Baldinger, Louis P. Dehner, D. Ashley Hill
The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer
Sofia Maia, Marta Cardoso, Paula Paulo, Manuela Pinheiro, Pedro Pinto, Catarina Santos, Carla Pinto, Ana Peixoto, Rui Henrique, Manuel R. Teixeira
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism
Laura Gigante, Irene Paganini, Marina Frontali, Serena Ciabattoni, Federica Carla Sangiuolo, Laura Papi
Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas
Ernst Näf, Dominik Laubscher, Helmut Hopfer, Markus Streit, Gabor Matyas
Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome
Francesco Tonelli, Carlo Biagini, Francesco Giudici, Federica Cioppi, Maria Luisa Brandi
Germline TERT promoter mutations are rare in familial melanoma
Mark Harland, Mia Petljak, Carla Daniela Robles-Espinoza, Zhihao Ding, Nelleke A. Gruis, Remco van Doorn, Karen A. Pooley, Alison M. Dunning, Lauren G. Aoude, Karin A. W. Wadt, Anne-Marie Gerdes, Kevin M. Brown, Nicholas K. Hayward, Julia A. Newton-Bishop, David J. Adams, D. Timothy Bishop
Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis
Jian Zhao, Xiaoyi Huang, Mingyuan Yang, Ming Li, Jianming Zheng