| 1 | MRBDT, SCWT, SMARCB1
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| Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1.
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| Swensen JJ, Keyser J, Coffin CM, Biegel JA, Viskochil DH, Williams MS.
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| J Med Genet 46(1):68-72.
2009
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| 2 | SMARCB1, SCWT
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| Germline Mutation of INI1/SMARCB1 in Familial Schwannomatosis.
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| Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P.
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| Am J Hum Genet 80(4):805-10. Epub 2007 Feb 16. 2007
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| 3 | SCWT, NF2
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| Familial schwannomatosis: exclusion of the NF2 locus as the germline event.
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| MacCollin M, Willett C, Heinrich B, Jacoby LB, Acierno JS Jr, Perry A, Louis DN.
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| Neurology 60(12):1968-74. 2003
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| 4 | NF2, SCWT
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| Somatic instability of the NF2 gene in schwannomatosis.
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| Kaufman DL, Heinrich BS, Willett C, Perry A, Finseth F, Sobel RA, MacCollin M.
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| Arch Neurol 60(9):1317-20. 2003
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| 5 | NF2, SCWT
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| A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene.
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| Bruder CE, et al.
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| Hum Genet 104(5):418-24. 1999
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| 6 | NF2, SCWT, TSG22A
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| Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis.
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| Jacoby LB, Jones D, Davis K, Kronn D, Short MP, Gusella J, MacCollin M.
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| Am J Hum Genet 61(6):1293-302. 1997
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| 7 | NF2, SCWT
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| Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study.
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| Evans DG, Mason S, Huson SM, Ponder M, Harding AE, Strachan T.
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| J Neurol Neurosurg Psychiatry 62(4):361-6. 1997
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| 8 | NF2, SCWT
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| Schwannomatosis: a clinical and pathologic study.
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| MacCollin M, et al.
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| Neurology 46(4):1072-9. Review. 1996
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