HuGE Literature Finder
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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 |
High-frequency type I/II mutational shifts between diagnosis and relapse are associated with outcome in pediatric AML: implications for personalized medicine. Blood 2010 Oct 116 (15): 2752-8. Bachas Costa, Schuurhuis Gerrit Jan, Hollink Iris H I M, Kwidama Zinia J, Goemans Bianca F, Zwaan C Michel, van den Heuvel-Eibrink Marry M, de Bont Eveline S J M, Reinhardt Dirk, Creutzig Ursula, de Haas Valerie, Assaraf Yehuda G, Kaspers Gertjan J L, Cloos Jacqueli |
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. Journal of the American Society of Nephrology : JASN 2010 Jul 21 (7): 1209-17. Machuca Eduardo, Benoit Geneviève, Nevo Fabien, Tête Marie-Josèphe, Gribouval Olivier, Pawtowski Audrey, Brandström Per, Loirat Chantal, Niaudet Patrick, Gubler Marie-Claire, Antignac Corin |
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