Volume 15; Issue 1

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Familial Cancer
Volume 15; Issue 1

Familial Cancer

Volume 15; Issue 1

1

Screening ofRETgene mutations in Chinese patients with medullary thyroid carcinoma and their relatives

Wang, Junyi, Zhang, Bin, Liu, Wensheng, Zhang, Yongxia, Di, Xuebing, Yang, Yanmei, Yan, Dangui

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 373 KB

english, 2016

2

Ovarian tumors related to intronic mutations inDICER1: a report from the international ovarian and testicular stromal tumor registry

Schultz, Kris Ann P., Harris, Anne, Messinger, Yoav, Sencer, Susan, Baldinger, Shari, Dehner, Louis P., Hill, D. Ashley

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 2.49 MB

english, 2016

3

The role of germline mutations in theBRCA1/2and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer

Maia, Sofia, Cardoso, Marta, Paulo, Paula, Pinheiro, Manuela, Pinto, Pedro, Santos, Catarina, Pinto, Carla, Peixoto, Ana, Henrique, Rui, Teixeira, Manuel R.

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 1.90 MB

english, 2016

4

Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects

Abdel-Malak, Camelia, Darwish, Hossam, Elsaid, Afaf, El-Tarapely, Fatma, Elshazli, Rami

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 415 KB

english, 2016

5

The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes

Amara, Nabil, Blouin-Bougie, Jolyane, Jbilou, Jalila, Halilem, Norrin, Simard, Jacques, Landry, Réjean

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 1.05 MB

english, 2016

6

Screening ofHELQin breast and ovarian cancer families

Pelttari, Liisa M., Kinnunen, Laura, Kiiski, Johanna I., Khan, Sofia, Blomqvist, Carl, Aittomäki, Kristiina, Nevanlinna, Heli

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 372 KB

english, 2016

7

First report of somatic mosaicism for mutations inSTK11in four patients with Peutz–Jeghers syndrome

McKay, Victoria, Cairns, Diane, Gokhale, David, Mountford, Roger, Greenhalgh, Lynn

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 837 KB

english, 2016

8

GermlineTERTpromoter mutations are rare in familial melanoma

Harland, Mark, Petljak, Mia, Robles-Espinoza, Carla Daniela, Ding, Zhihao, Gruis, Nelleke A., van Doorn, Remco, Pooley, Karen A., Dunning, Alison M., Aoude, Lauren G., Wadt, Karin A. W., Gerdes, Anne-

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 442 KB

english, 2016

9

Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer?

Chikman, Bar, Davidson, Tima, Kais, Hasan, Jeroukhimov, Igor, Leshno, Ari, Sandbank, Judith, Halevy, Ariel, Lavy, Ron

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 390 KB

english, 2016

10

Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome

Tonelli, Francesco, Biagini, Carlo, Giudici, Francesco, Cioppi, Federica, Brandi, Maria Luisa

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 972 KB

english, 2016

11

Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned

Duong, Bich-Thu, Savarirayan, Ravi, Winship, Ingrid

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 868 KB

english, 2016

12

Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study

Matsumoto, Minori, Nakajima, Takeshi, Kakugawa, Yasuo, Sakamoto, Taku, Kuribayashi, Shiko, Otake, Yosuke, Matsuda, Takahisa, Kanemitsu, Yukihide, Taniguchi, Hirokazu, Saito, Yutaka

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 740 KB

english, 2016

13

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

Quast, Daniel Robert, Schneider, Ralph, Burdzik, Emanuel, Hoppe, Steffen, Möslein, Gabriela

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 465 KB

english, 2016

14

Birt–Hogg–Dubé syndrome: novelFLCNframeshift deletion in daughter and father with renal cell carcinomas

Näf, Ernst, Laubscher, Dominik, Hopfer, Helmut, Streit, Markus, Matyas, Gabor

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 985 KB

english, 2016

15

Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis

Zhao, Jian, Huang, Xiaoyi, Yang, Mingyuan, Li, Ming, Zheng, Jianming

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 874 KB

english, 2016

16

Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism

Gigante, Laura, Paganini, Irene, Frontali, Marina, Ciabattoni, Serena, Sangiuolo, Federica Carla, Papi, Laura

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 1.60 MB

english, 2016

17

Genetic testing for Lynch syndrome: family communication and motivation

Leenen, Celine H. M., Heijer, Mariska den, van der Meer, Conny, Kuipers, Ernst J., van Leerdam, Monique E., Wagner, Anja

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 458 KB

english, 2016

18

Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary

Papp, Janos, Kovacs, Marietta Eva, Matrai, Zoltan, Orosz, Enikő, Kásler, Miklós, Børresen-Dale, Anne-Lise, Olah, Edith

Journal:

Familial Cancer

Year:

2016

Language:

english

File:

PDF, 1.32 MB

english, 2016