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Cancer Genetics|June 22, 2021
Molecular follow-up of first-line treatment by osimertinib in lung cancer: Importance of using appropriate tools for detecting EGFR resistance mutation C797SY Fanjat, H Barazzutti, I Di Mauro, et al.Cancer Genetics|June 21, 2021
Whole-exome sequencing in osteosarcoma with distinct prognosis reveals disparate genetic heterogeneityWeifeng Liu, Renxian Wang, Yanrui Zhang, et al.Cancer Genetics|July 5, 2021
A pediatric BAL case with double Ph chromosomes and trisomy 5Gulcin Gunden, Sevgi Isik, Canan Ozdemir, et al.Cancer Genetics|June 13, 2021
A hereditary ovarian cancer family with rare pathogenic splicing mutation: Implications for variant interpretationKe Wang, Yingnan Ye, Lewen Bao, et al.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.Pageof 114