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注意：仅列出部分参考文献，下载原文获取全部文献信息。SMARCB1 mutations are not a common cause of multiple meningiomas
K. D. Hadfield et al.
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An update on age related mosaic and offspring risk in neurofibromatosis 2 (NF2)
D. G. R. Evans et al.
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What are the implications in individuals with unilateral vestibular schwannoma and other neurogenic tumors?
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Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis
K. D. Hadfield et al.
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Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplification
Gareth R. Evans et al.
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Should NF2 mutation screening be undertaken in patients with an apparently isolated vestibular schwannoma?
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CLINICAL GENETICS (2007)
Diagnostic criteria for schwannomatosis
M MacCollin et al.
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Spinal tumors in neurofibromatosis Type 2. Is emerging knowledge of genotype predictive of natural history?
G Dow et al.
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Management of the patient and family with neurofibromatosis 2: a consensus conference statement
DGR Evans et al.
BRITISH JOURNAL OF NEUROSURGERY (2005)
Multiple meningiomas: differential involvement of the NF2 gene in children and adults
DGR Evans et al.
JOURNAL OF MEDICAL GENETICS (2005)
Presymptomatic diagnosis for children of sporadic neurofibromatosis 2 patients: A method based on tumor analysis
L Kluwe et al.
GENETICS IN MEDICINE (2002)
Use of MRI and audiological tests in presymptomatic diagnosis of type 2 neurofibromatosis (NF2)
DGR Evans et al.
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