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Cancer Genetics|October 26, 2022
Partial tandem duplication of KMT2A gene in patient afflicted with hypereosinophilic syndrome: A case reportFaramarz Ghasemian Sorbeni, Atefeh Ansarin, Ebrahim Sakhinia, et al.
Cancer Genetics|October 24, 2022
Myxoid spindle cell sarcoma with ETV6-NTRK3 fusionAnastasios Kyriazoglou, Efhtymios Dimitriadis, Luiza Mahaira, et al.
Cancer Genetics|September 30, 2021
Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genesRunjun D Kumar, Briana A Burns, Paul J Vandeventer, et al.
Cancer Genetics|February 26, 2022
Cancer risk among RECQL4 heterozygotesBailey A Martin-Giacalone, Ta-Tara Rideau, Michael E Scheurer, et al.
Cancer Genetics|February 2, 2022
The promise of TRK inhibitors in pediatric cancers with NTRK fusionsEmily R Blauel, Theodore W Laetsch
Cancer Genetics|March 30, 2022
Functional analysis of ATM variants in a high risk cohort provides insight into missing heritabilityScott L Baughan, Fatima Darwiche, Michael A Tainsky
Cancer Genetics|March 15, 2022
NTRK-fusions in pediatric thyroid tumors: Current state and future perspectivesVictoria Casado-Medrano, Alison O'Neill, Stephen Halada, et al.
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