HuGE Literature Finder
Records
1
-
5
Novel combined variants of WT1 and TET2 in a refractory and recurrent AML patient. BMC medical genomics 2021 (1): 158. Ma Qiang, Guo Yixian, Lan Xiaoxi, Wang Guoxiang, Sun Wanli |
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 |
The assessment of minimal residual disease versus that of somatic mutations for predicting the outcome of acute myeloid leukemia patients. Cancer cell international 2019 19 83. Salehzadeh Serena, Guerrini Francesca, Pizzano Umberto, Grassi Susanna, Ciabatti Elena, Iovino Lorenzo, Buda Gabriele, Caracciolo Francesco, Benedetti Edoardo, Orciuolo Enrico, Pelosini Matteo, Consani Giovanni, Carulli Giovanni, Metelli Maria Rita, Martini Francesca, Mazziotta Francesco, Mazzantini Elisa, Rossi Pietro, Tavarozzi Rita, Ricci Federica, Petrini Mario, Galimberti Sa |
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients. Clinical nephrology 2012 Jul 78 (1): 47-53. Büscher Anja K, Konrad Martin, Nagel Mato, Witzke Oliver, Kribben Andreas, Hoyer Peter F, Weber Stefan |
Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia: a study from the Acute Leukemia French Association. Cancer 2009 Jun . Renneville A, Boissel N, Zurawski V, Llopis L, Biggio V, Nibourel O, Philippe N, Thomas X, Dombret H, Preudhomme C |
- Page last reviewed:Feb 1, 2023
- Page last updated:Feb 03, 2023
- Content source: