Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Leukemia and TBL1XR1[original query] |
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Key pathways are frequently mutated in high-risk childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group. Blood 2011 Sep 118 (11): 3080-7. Zhang Jinghui, Mullighan Charles G, Harvey Richard C, Wu Gang, Chen Xiang, Edmonson Michael, Buetow Kenneth H, Carroll William L, Chen I-Ming, Devidas Meenakshi, Gerhard Daniela S, Loh Mignon L, Reaman Gregory H, Relling Mary V, Camitta Bruce M, Bowman W Paul, Smith Malcolm A, Willman Cheryl L, Downing James R, Hunger Stephen |
Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011. Leukemia 2014 Feb 28 (2): 302-10. Olsson L, Castor A, Behrendtz M, Biloglav A, Forestier E, Paulsson K, Johansson |
MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations. American journal of human genetics 2016 Feb . Hua Xing, Hyland Paula L, Huang Jing, Song Lei, Zhu Bin, Caporaso Neil E, Landi Maria Teresa, Chatterjee Nilanjan, Shi Jianx |
The genetics and clinical characteristics of children morphologically diagnosed as acute promyelocytic leukemia. Leukemia 2019 Jun 33 (6): 1387-1399. Zhao Jie, Liang Jian-Wei, Xue Hui-Liang, Shen Shu-Hong, Chen Jing, Tang Yan-Jing, Yu Li-Sha, Liang Huan-Huan, Gu Long-Jun, Tang Jing-Yan, Li Ben-Sha |
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