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Cancer Genetics|May 8, 2012
Partial trisomy of chromosome 13 as a single cytogenetic abnormality in an Italian case of nasal NK/T lymphomaSilvia Uccella, Barbara Bernasconi, Isabella Ricotti, et al.Cancer Genetics|May 21, 2018
Clinical germline diagnostic exome sequencing for hereditary cancer: Findings within novel candidate genes are prevalentZöe Powis, Carin R Espenschied, Holly LaDuca, et al.Cancer Genetics|May 21, 2018
Nuclear BAP1 loss is common in intrahepatic cholangiocarcinoma and a subtype of hepatocellular carcinoma but rare in pancreatic ductal adenocarcinomaAsmaa Mosbeh, Khalil Halfawy, Wael S Abdel-Mageed, et al.Cancer Genetics|June 10, 2017
Recurrent large genomic rearrangements in BRCA1 and BRCA2 in an Irish case seriesTerri P McVeigh, Nuala Cody, Cliona Carroll, et al.Cancer Genetics|April 29, 2017
Gene fusions PAFAH1B1-USP6 and RUNX2-USP6 in aneurysmal bone cysts identified by next generation sequencingMikako Warren, Dongbin Xu, Xia LiCancer Genetics|April 19, 2018
Biallelic TP53 gain of function mutations in rapidly progressing solid tumorsChristopher M Sande, Brian Chang, Varun Monga, et al.Cancer Genetics|April 19, 2018
Mutation analysis of therapy-related myeloid neoplasmsTakahiro Nishiyama, Yuichi Ishikawa, Naomi Kawashima, et al.Cancer Genetics|April 19, 2018
H2AFY is a novel fusion partner of MECOM in acute myeloid leukemiaQiaoyan Han, Jiao Lu, Jianjiang Wang, et al.Cancer Genetics|October 3, 2012
An optimized technology platform for the rapid multiplex molecular analysis of genetic alterations associated with leukemiaFei Ye, Walairat Laosinchai-Wolf, Emmanuel LabourierCancer Genetics|August 18, 2020
Identification of diagnostic DNA methylation biomarkers specific for early-stage lung adenocarcinomaQidong Cai, Pengfei Zhang, Boxue He, et al.Pageof 113