Ausgabe 4/2011
“The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer” Delta Centre-Ville Hotel, Montreal, Quebec, Canada, October 10-11, 2011
Inhalt (14 Artikel)
Familial colorectal cancer type X syndrome: two distinct molecular entities?
Inês Francisco, Cristina Albuquerque, Pedro Lage, Hélio Belo, Inês Vitoriano, Bruno Filipe, Isabel Claro, Sara Ferreira, Paula Rodrigues, Paula Chaves, Carlos Nobre Leitão, António Dias Pereira
Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study
Helle Vendel Petersen, Mary Jane Esplen, Steen Ladelund, Inge Bernstein, Lone Sunde, Christina Carlsson, Mef Nilbert
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals
Mev Dominguez Valentin, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, Bianca Garcia Lisboa, Ligia Petrolini de Oliveira, Fabio de Oliveira Ferreira, Israel Gomy, Wilson Toshihiko Nakagawa, Samuel Aguiar Junior, Mariana Redal, Carlos Vaccaro, Adriana Della Valle, Carlos Sarroca, Dirce Maria Carraro, Benedito Mauro Rossi
Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment
Noriko Ishii, Masami Arai, Yurie Koyama, Masashi Ueno, Toshiharu Yamaguchi, Keiko Kazuma, Tetsuichiro Muto
Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome
Julie Bouquier, Hélène Blons, Céline Narjoz, Fabrice Lécuru, Pierre Laurent-Puig, Anne-Sophie Bats
A survey of APC mutations in Quebec
Jonathan Jarry, Jean-Sébastien Brunet, Rachel Laframboise, Régen Drouin, Jean Latreille, Carole Richard, Jean Gekas, Bruno Maranda, Yury Monczak, Nora Wong, Carly Pouchet, Sonya Zaor, Lidia Kasprzak, Laura Palma, Mona Kay Wu, Marc Tischkowitz, William D. Foulkes, George Chong
The identification and management of hereditary diffuse gastric cancer in a large Jordanian family
Henry T. Lynch, Ibrahim Aldoss, Jane F. Lynch
Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care center
K. Ready, B. K. Arun, K. M. Schmeler, A. Uyei, J. K. Litton, K. H. Lu, C. C. Sun, S. K. Peterson
Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints
Noriko Ando, Yumi Iwamitsu, Masaru Kuranami, Shigemi Okazaki, Kenji Yamamoto, Masahiko Watanabe, Hitoshi Miyaoka
Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?
Hugo Villeneuve, Steve Tremblay, Polymnia Galiatsatos, Nancy Hamel, Louis Guertin, Renald Morency, Marc Tischkowitz
Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors
Wai Kwan Siu, Chun Yiu Law, Ching Wan Lam, Chloe Miu Mak, Gary Wing Kin Wong, Andrew Yiu Yan Ho, Kwok Yip Ho, Ka Tai Loo, Sin Chuen Chiu, Louis Tsun Cheung Chow, Sui Fan Tong, Albert Yan Wo Chan
Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A
Sarah M. Nielsen, Wendy S. Rubinstein, Darcy L. Thull, Michaele J. Armstrong, Eleanor Feingold, Linwah Yip, Samuel A. Tisherman, Sally E. Carty
Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan
Muhammad U. Rashid, Sidra Gull, Saima Faisal, Saba Khaliq, Kashif Asghar, Neelam Siddiqui, Asim Amin, Ute Hamann