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The Lancet. Child & Adolescent Health|March 20, 2019
Identification of new Wilms tumour predisposition genes: an exome sequencing studyShazia Mahamdallie, Shawn Yost, Emma Poyastro-Pearson, et al.
NMR in Biomedicine|March 25, 2015
Multi-centre reproducibility of diffusion MRI parameters for clinical sequences in the brainMatthew Grech-Sollars, Patrick W Hales, Keiko Miyazaki, et al.
Blood Advances|September 16, 2022
Lineage switching of the cellular distribution of BRAFV600E in multisystem Langerhans cell histiocytosisPaul Milne, Simon Bomken, Olga Slater, et al.
Nature Genetics|March 10, 2009
Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastomaPaul A Northcott, Yukiko Nakahara, Xiaochong Wu, et al.
Acta Neuropathologica|June 18, 2018
Molecular heterogeneity and CXorf67 alterations in posterior fossa group A (PFA) ependymomasKristian W Pajtler, Ji Wen, Martin Sill, et al.
Acta Neuropathologica|May 21, 2014
CNS-PNETs with C19MC amplification and/or LIN28 expression comprise a distinct histogenetic diagnostic and therapeutic entityTara Spence, Patrick Sin-Chan, Daniel Picard, et al.
Elife|October 2, 2014
Origins and functional consequences of somatic mitochondrial DNA mutations in human cancerYoung Seok Ju, Ludmil B Alexandrov, Moritz Gerstung, et al.
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