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23. Association of PDGFRB Mutations With Pediatric Myofibroma and Myofibromatosis. Dachy G, de Krijger RR, Fraitag S, Théate I, Brichard B, Hoffman SB, Libbrecht L, Arts FA, Brouillard P, Vikkula M, Limaye N, Demoulin JB. JAMA Dermatol; 2019 Aug 01; 155(8):946-950. PubMed ID: 31017643 [Abstract] [Full Text] [Related]
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28. Identification and functional characterization of imatinib-sensitive DTD1-PDGFRB and CCDC88C-PDGFRB fusion genes in eosinophilia-associated myeloid/lymphoid neoplasms. Gosenca D, Kellert B, Metzgeroth G, Haferlach C, Fabarius A, Schwaab J, Kneba M, Scheid C, Töpelt K, Erben P, Haferlach T, Cross NC, Hofmann WK, Seifarth W, Reiter A. Genes Chromosomes Cancer; 2014 May 11; 53(5):411-21. PubMed ID: 24772479 [Abstract] [Full Text] [Related]
29. Treatment of generalized infantile myofibromatosis with sorafenib and imatinib: A case report. Bidadi B, Watson A, Weigel B, Oliveira A, Kirkham J, Arndt C. Pediatr Blood Cancer; 2020 Jun 11; 67(6):e28288. PubMed ID: 32307894 [Abstract] [Full Text] [Related]
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34. Mutations in PDGFRB and NOTCH3 are the first genetic causes identified for autosomal dominant infantile myofibromatosis. Lee JW. Clin Genet; 2013 Oct 11; 84(4):340-1. PubMed ID: 23865785 [No Abstract] [Full Text] [Related]
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