Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Neurofibromatosis 2 and SMARCB1[original query] |
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| SMARCB1 mutations are not a common cause of multiple meningiomas. Journal of medical genetics 2010 Aug 47 (8): 567-8. Hadfield K D, Smith M J, Trump D, Newman W G, Evans D |
| Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young Adults. JAMA neurology 2017 8 74 (9): 1123-1129. Pathmanaban Omar N, Sadler Katherine V, Kamaly-Asl Ian D, King Andrew T, Rutherford Scott A, Hammerbeck-Ward Charlotte, McCabe Martin G, Kilday John-Paul, Beetz Christian, Poplawski Nicola K, Evans D Gareth, Smith Miriam |
| Pathogenic noncoding variants in the neurofibromatosis and schwannomatosis predisposition genes. Human mutation 2021 7 42 (10): 1187-1207. Perez-Becerril Cristina, Evans D Gareth, Smith Miriam |
| Malignant peripheral nerve sheath tumor in children: A clinicopathologic and molecular study with parallels to the adult counterpart. Genes, chromosomes & cancer 2022 11 62 (3): 131-138. Agaram Narasimhan P, Wexler Leonard H, Chi Ping, Antonescu Cristina |
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