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Cancer Genetics|June 11, 2021
Long-read nanopore sequencing enables accurate confirmation of a recurrent PMS2 insertion-deletion variant located in a region of complex genomic architectureChristopher M Watson, Laura A Crinnion, Jennifer Simmonds, et al.Cancer Genetics|May 21, 2018
ETV6/RUNX1-positive childhood acute lymphoblastic leukemia (ALL): The spectrum of clonal heterogeneity and its impact on prognosisM Ampatzidou, S I Papadhimitriou, G Paterakis, et al.Cancer Genetics|May 21, 2018
EGFL7 and RASSF1 promoter hypermethylation in epithelial ovarian cancerYanisa Rattanapan, Veerawat Korkiatsakul, Adcharee Kongruang, et al.Cancer Genetics|July 15, 2018
Differentially expressed LncRNAs as potential prognostic biomarkers for glioblastomaMei Shao, Wenyun Liu, Yu WangCancer Genetics|April 19, 2018
Deletion of RUNX1 exons 1 and 2 associated with familial platelet disorder with propensity to acute myeloid leukemiaMarcela Cavalcante de Andrade Silva, Ana Cristina Victorino Krepischi, Leslie Domenici Kulikowski, et al.Cancer Genetics|June 4, 2019
Acute lymphoblastic leukemia in a nine-year-old girl with isodicentric chromosome 15 syndromeRoberto Antonucci, Nadia Vacca, Elisa Ghisu, et al.Cancer Genetics|May 22, 2019
Deciphering the complexities of MECOM rearrangement-driven chromosomal aberrationsZhenya Tang, Guilin Tang, Shimin Hu, et al.Cancer Genetics|May 7, 2019
Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testingThomas P Slavin, Bradford Coffee, Ryan Bernhisel, et al.Cancer Genetics|May 13, 2019
Uptake of genetic testing for germline BRCA1/2 pathogenic variants in a predominantly Hispanic populationJulia E McGuinness, Meghna S Trivedi, Thomas Silverman, et al.Cancer Genetics|March 20, 2022
Evolution of germline TP53 variant classification in children with cancerE Tallis, S Scollon, D I Ritter, et al.Pageof 113