| 1 | MRBDT, SMARCB1
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| SMARCB1 Deficiency in Tumors From the Peripheral Nervous System: A Link Between Schwannomas and Rhabdoid Tumors?
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| Rizzo D, Fréneaux P, Brisse H, Louvrier C, Lequin D, Nicolas A, Ranchère D, Verkarre V, Jouvet A, Dufour C, Edan C, Stéphan JL, Orbach D, Sarnacki S, Pierron G, Parfait B, Peuchmaur M, Delattre O, Bourdeaut F.
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| Am J Surg Pathol 36(7):964-972.
2012
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| 2 | 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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| 3 | MRBDT, SMARCB1, TSG22D
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| Constitutional Mutations of the hSNF5/INI1 Gene Predispose to a Variety of Cancers.
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| Sevenet N, Sheridan E, Amram D, Schneider P, Handgretinger R, Delattre O.
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| Am J Hum Genet 65(5):1342-1348 1999
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| 4 | MRBDT, SMARCB1
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| Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations.
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| Sevenet N, Lellouch-Tubiana A, Schofield D, Hoang-Xuan K, Gessler M, Birnbaum D, Jeanpierre C, Jouvet A, Delattre O.
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| Hum Mol Genet 8(13):2359-68 1999
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