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Cancer Genetics|April 26, 2021
Late recurrence of lung adenocarcinoma harboring EGFR exon 20 insertion (A763_Y764insFQEA) mutation successfully treated with osimertinibKei Kunimasa, Kazumi Nishino, Yoji Kukita, et al.
Cancer Genetics|April 18, 2021
The spectrum of tumors harboring BAP1 gene alterationsYael Laitman, Justin Newberg, Rinat Bernstein Molho, et al.
Cancer Genetics|October 16, 2012
Acute myeloid leukemia presenting in a mother and daughter pair with the identical acquired karyotypic abnormality consisting of inversion 3q21q26 and monosomy 7: a review of possible mechanismsAlastair Lawrie, David A J Stevenson, Tamasin N Doig, et al.
Cancer Genetics|June 5, 2014
Malignant rhabdoid tumor of the liver presented with initial tumor ruptureDenis Kachanov, Margarita Teleshova, Eduard Kim, et al.
Cancer Genetics|January 7, 2014
Multiple EWSR1-WT1 and WT1-EWSR1 copies in two cases of desmoplastic round cell tumorRoberta La Starza, Gianluca Barba, Valeria Nofrini, et al.
Cancer Genetics|January 7, 2014
Design of targeted, capture-based, next generation sequencing tests for precision cancer therapyIan S Hagemann, Catherine E Cottrell, Christina M Lockwood
Cancer Genetics|February 16, 2015
Hypermethylation of the CpG dinucleotide in epidermal growth factor receptor codon 790: implications for a mutational hotspot leading to the T790M mutation in non-small-cell lung cancerAkiko Fujii, Taishi Harada, Eiji Iwama, et al.
Cancer Genetics|February 17, 2015
A functional variant in miR-605 modifies the age of onset in Li-Fraumeni syndromeBadr Id Said, David Malkin
Cancer Genetics|April 7, 2015
Molecular studies reveal a MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotypeDaniela Ribeiro Ney Garcia, Thomas Liehr, Mariana Emerenciano, et al.
Cancer Genetics|July 5, 2020
Clinical exome sequencing identified POLB c.C1002A as a possible genetic cause in a family with hereditary cancer-predisposing syndromeZhenxin Zhu, Jieshi Wang, Lisha Jiang, et al.
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