Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Monosomy and IDH1[original query] |
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Distinct clinical and biologic characteristics in adult acute myeloid leukemia bearing the isocitrate dehydrogenase 1 mutation. Blood 2010 Apr 115 (14): 2749-54. Chou Wen-Chien, Hou Hsin-An, Chen Chien-Yuan, Tang Jih-Luh, Yao Ming, Tsay Woei, Ko Bor-Shen, Wu Shang-Ju, Huang Shang-Yi, Hsu Szu-Chun, Chen Yao-Chang, Huang Yen-Ning, Chang Yi-Chang, Lee Fen-Yu, Liu Ming-Chi, Liu Chia-Wen, Tseng Mei-Hsuan, Huang Chi-Fei, Tien Hwei-Fa |
Granular cell astrocytoma: an aggressive IDH-wildtype diffuse glioma with molecular genetic features of primary glioblastoma. Brain pathology (Zurich, Switzerland) 2018 Sep . Vizcaino M Adelita, Palsgrove Doreen N, Yuan Ming, Giannini Caterina, Cabrera-Aldana Eibar Ernesto, Pallavajjala Aparna, Burger Peter C, Rodriguez Fausto |
ASXL1 and STAG2 are common mutations in GATA2 deficiency patients with bone marrow disease and myelodysplastic syndrome. Blood advances 2021 9 6 (3): 793-807. West Robert R, Calvo Katherine R, Embree Lisa J, Wang Weixin, Tuschong Laura M, Bauer Thomas R, Tillo Desiree, Lack Justin, Droll Stephenie, Hsu Amy P, Holland Steven M, Hickstein Dennis |
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- Page last updated:Sep 18, 2023
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