Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Wilms Tumor and KRAS[original query] |
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Clinical significance of hypermethylation status in NSCLC: evaluation of a 30-gene panel in patients with advanced disease. Anticancer research 2011 Dec 31 (12): 12. Pesek M, Kopeckova M, Benesova L, Meszarosova A, Mukensnabl P, Bruha F, Minarik M |
WT1 mutation in pediatric patients with acute myeloid leukemia: a report from the Japanese Childhood AML Cooperative Study Group. International journal of hematology 2013 Oct 98 (4): 437-45. Sano Hirozumi, Shimada Akira, Tabuchi Ken, Taki Tomohiko, Murata Chisato, Park Myoung-ja, Ohki Kentaro, Sotomatsu Manabu, Adachi Souichi, Tawa Akio, Kobayashi Ryoji, Horibe Keizo, Tsuchida Masahiro, Hanada Ryoji, Tsukimoto Ichiro, Hayashi Yasuhi |
Clinical, Pathologic, and Genetic Features of Wilms Tumors With WTX Gene Mutation. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 0 20 (2): 105-111. Alexandrescu Sanda, Akhavanfard Sara, Harris Marian H, Vargas Sara |
Association of KRAS and NRAS gene polymorphisms with Wilms tumor risk: a four-center case-control study. Aging 2019 3 11 (5): 1551-1563. Fu Wen, Zhuo Zhenjian, Hua Rui-Xi, Fu Kai, Jia Wei, Zhu Jinhong, Zhang Jiao, Cheng Jiwen, Zhou Haixia, Xia Huimin, He Jing, Liu Guocha |
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