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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 8, 2023. (Total: 223870Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Neurofibromatosis 2 and SMARCB1[original query]
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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