Targetable molecular alterations in congenital glioblastoma
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Clinical Neurology,Neurology,Oncology
Link
http://link.springer.com/content/pdf/10.1007/s11060-019-03377-8.pdf
Reference31 articles.
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3. Cocce MC, Mardin BR, Bens S, Stutz AM, Lubieniecki F, Vater I, Korbel JO, Siebert R, Alonso CN, Gallego MS (2016) Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3). Genes Chromosom Cancer 55:677–687. https://doi.org/10.1002/gcc.22369
4. Isaacs H Jr (2016) Perinatal (fetal and neonatal) astrocytoma: a review. Childs Nerv Syst 32:2085–2096. https://doi.org/10.1007/s00381-016-3215-y
5. Kameda M, Otani Y, Ichikawa T, Shimada A, Ichimura K, Date I (2017) Congenital glioblastoma with distinct clinical and molecular characteristics: case reports and a literature review. World Neurosurg 101:817. https://doi.org/10.1016/j.wneu.2017.02.026
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