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2. Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor. Thomas C; Oehl-Huber K; Bens S; Soschinski P; Koch A; Nemes K; Oyen F; Kordes U; Kool M; Frühwald MC; Hasselblatt M; Siebert R Genes Chromosomes Cancer; 2021 Aug; 60(8):586-590. PubMed ID: 33896072 [TBL] [Abstract][Full Text] [Related]
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6. Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases. Holdhof D; Johann PD; Spohn M; Bockmayr M; Safaei S; Joshi P; Masliah-Planchon J; Ho B; Andrianteranagna M; Bourdeaut F; Huang A; Kool M; Upadhyaya SA; Bendel AE; Indenbirken D; Foulkes WD; Bush JW; Creytens D; Kordes U; Frühwald MC; Hasselblatt M; Schüller U Acta Neuropathol; 2021 Feb; 141(2):291-301. PubMed ID: 33331994 [TBL] [Abstract][Full Text] [Related]
7. Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors. Sabatella M; Mantere T; Waanders E; Neveling K; Mensenkamp AR; van Dijk F; Hehir-Kwa JY; Derks R; Kwint M; O'Gorman L; Tropa Martins M; Gidding CE; Lequin MH; Küsters B; Wesseling P; Nelen M; Biegel JA; Hoischen A; Jongmans MC; Kuiper RP J Pathol; 2021 Oct; 255(2):202-211. PubMed ID: 34231212 [TBL] [Abstract][Full Text] [Related]
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10. Concurrent myeloid sarcoma, atypical teratoid/rhabdoid tumor, and hypereosinophilia in an infant with a germline SMARCB1 mutation. Metts JL; Park SI; Soares BP; Fong C; Biegel JA; Goldsmith KC Pediatr Blood Cancer; 2017 Sep; 64(9):. PubMed ID: 28111898 [TBL] [Abstract][Full Text] [Related]
11. Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism. Gigante L; Paganini I; Frontali M; Ciabattoni S; Sangiuolo FC; Papi L Fam Cancer; 2016 Jan; 15(1):123-6. PubMed ID: 26342593 [TBL] [Abstract][Full Text] [Related]
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13. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22. Byers HM; Adam MP; LaCroix A; Leary SE; Cole B; Dobyns WB; Mefford HC Am J Med Genet A; 2017 Jan; 173(1):245-249. PubMed ID: 27734605 [TBL] [Abstract][Full Text] [Related]
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