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Cancer Genetics|December 3, 2014
Concurrence of B-lymphoblastic leukemia and myeloproliferative neoplasm with copy neutral loss of heterozygosity at chromosome 1p harboring a MPL W515S mutationJiangchuan Tao, Xiaohui Zhang, Jeffrey Lancet, et al.
Cancer Genetics|December 3, 2014
Genomic microarray analysis on formalin-fixed paraffin-embedded material for uveal melanoma prognosticationEugen C Minca, Raymond R Tubbs, Bryce P Portier, et al.
Cancer Genetics|November 19, 2020
How to structure an oncogenetics service for the public health system: Report of the implementation of the first service in Northeastern BrazilCamila Sampaio Nogueira, Isabelle Joyce de Lima Silva-Fernandes, Clarissa Gondim Picanço de Albuquerque, et al.
Cancer Genetics|November 13, 2020
FANCA, TP53, and del(5q)/RPS14 alterations in a patient with T-cell non-Hodgkin lymphoma and concomitant Fanconi anemia and Li-Fraumeni syndromeEdoardo Errichiello, Tommaso Mina, Patrizia Morbini, et al.
Cancer Genetics|January 22, 2020
hsa_circ_0062389 promotes the progression of non-small cell lung cancer by sponging miR-103a-3p to mediate CCNE1 expressionYahui She, Yuanyuan Han, Guangting Zhou, et al.
Cancer Genetics|November 4, 2019
High-resolution copy number analysis of clear cell endometrial carcinomaAndrea J O'Hara, Matthieu Le Gallo, Meghan L Rudd, et al.
Cancer Genetics|February 7, 2018
SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)Sarah H Johnson, James B Smadbeck, Stephanie A Smoley, et al.
Cancer Genetics|February 7, 2018
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasmRoberto R Capela de Matos, Moneeb A K Othman, Gerson M Ferreira, et al.
Cancer Genetics|February 7, 2018
Survey of gynecological carcinosarcomas in families with breast and ovarian cancer predispositionCarla B Ripamonti, Siranoush Manoukian, Bernard Peissel, et al.
Cancer Genetics|January 10, 2018
A leukemic double-hit follicular lymphoma associated with a complex variant translocation, t(8;14;18)(q24;q32;q21), involving BCL2, MYC, and IGHDaisuke Minakata, Kazuya Sato, Takashi Ikeda, et al.
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