Lynch syndrome|https://phgkb.cdc.gov/GAPPKB/phgHome.do|Lynch syndrome

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Molecular Testing for Gastrointestinal Cancer.  
  Journal of pathology and translational medicine 2017 Feb .
  Lee Hye Seung, Kim Woo Ho, Kwak Yoonjin, Koh Jiwon, Bae Jeong Mo, Kim Kyoung-Mee, Chang Mee Soo, Han Hye Seung, Kim Joon Mee, Kim Hwal Woong, Chang Hee Kyung, Choi Young Hee, Park Ji Y, Gu Mi Jin, Lhee Min Jin, Kim Jung Yeon, Kim Hee Sung, Cho Mee-Yon, ,
• Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.  
  Journal of molecular medicine (Berlin, Germany) 2017 Jan .
  Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia
• [Lynch syndrome, Muir Torre variant: 2 cases].  
  Rev Gastroenterol Peru 2016 Jan-Mar (36): 81-5.
  Castro-Mujica María Del Carmen, Barletta-Carrillo Claudia, Acosta-Aliaga Marisa, Montenegro-Garreaud Xime
• [Evaluation of BRAF V600E Mutations in High-Level Microsatellite Instability(MSI-H)Colon Cancer - Comparison Between Genetic Testing and Immunohistochemical Staining].  
  Gan to kagaku ryoho. Cancer & chemotherapy 2016 Nov 43 (12): 1693-1695.
  Sakimoto Takehiko, Chika Noriyasu, Suzuki Okihide, Ishibashi Keiichiro, Tachikawa Tetsuhiko, Akagi Kiwamu, Eguchi Hidetaka, Okazaki Yasushi, Ishida Hideyu
• Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients.  
  Cancer genetics 2016 Nov 209 (11): 497-500.
  Liu Qing, Hesson Luke B, Nunez Andrea C, Packham Deborah, Hawkins Nicholas J, Ward Robyn L, Sloane Mathew

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