Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Disease Progression and WT1[original query] |
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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 |
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 |
Case Report: A Pathogenic Missense Variant of WT1 Cosegregates With Proteinuria in a Six-Generation Chinese Family With IgA Nephropathy. Frontiers in medicine 2022 2 8 810940. Li Qianqian, Zhu Li, Shi Sufang, Xu Damin, Lv Jicheng, Zhang Ho |
NEXT-GENERATION SEQUENCING-BASED GENOMIC PROFILING OF CHILDREN WITH ACUTE MYELOID LEUKEMIA. The Journal of molecular diagnostics : JMD 2023 4 . Szilvia Krizsán, Borbála Péterffy, Bálint Egyed, Tibor Nagy, Endre Sebestyén, Lajos László Hegyi, Zsuzsanna Jakab, Dániel J Erdélyi, Judit Müller, György Péter, Krisztina Csanádi, Krisztián Kállay, Gergely Kriván, Gábor Barna, Gábor Bedics, Irén Haltrich, Gábor Ottóffy, Katalin Csernus, Ágnes Vojcek, Lilla Györgyi Tiszlavicz, Krisztina Mita Gábor, Ágnes Kelemen, Péter Hauser, Zsuzsanna Gaál, István Szegedi, Anikó Ujfalusi, Béla Kajtár, Csongor Kiss, András Matolcsy, Botond Tímár, Gábor Kovács, Donát Alpár, Csaba Böd |
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