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Cited In for PMID: 27055474

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Germline RRAS2 mutations are not associated with Noonan syndrome.
Ceremsak JJ, Yu A, Esquivel E, Lissewski C, Zenker M, Loh ML, Stieglitz E. Ceremsak JJ, et al. J Med Genet. 2016 Nov;53(11):728. doi: 10.1136/jmedgenet-2016-103889. Epub 2016 Apr 7. J Med Genet. 2016. PMID: 27055474 No abstract available.
EAHP 2020 workshop proceedings, pediatric myeloid neoplasms.
Leguit RJ, Orazi A, Kucine N, Kvasnicka HM, Gianelli U, Arber DA, Porwit A, Ponzoni M. Leguit RJ, et al. Virchows Arch. 2022 Oct;481(4):621-646. doi: 10.1007/s00428-022-03375-8. Epub 2022 Jul 11. Virchows Arch. 2022. PMID: 35819517 Free PMC article.
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome.
Capri Y, Flex E, Krumbach OHF, Carpentieri G, Cecchetti S, Lißewski C, Rezaei Adariani S, Schanze D, Brinkmann J, Piard J, Pantaleoni F, Lepri FR, Goh ES, Chong K, Stieglitz E, Meyer J, Kuechler A, Bramswig NC, Sacharow S, Strullu M, Vial Y, Vignal C, Kensah G, Cuturilo G, Kazemein Jasemi NS, Dvorsky R, Monaghan KG, Vincent LM, Cavé H, Verloes A, Ahmadian MR, Tartaglia M, Zenker M. Capri Y, et al. Am J Hum Genet. 2019 Jun 6;104(6):1223-1232. doi: 10.1016/j.ajhg.2019.04.013. Epub 2019 May 23. Am J Hum Genet. 2019. PMID: 31130282 Free PMC article.
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children.
de Smith AJ, Lavoie G, Walsh KM, Aujla S, Evans E, Hansen HM, Smirnov I, Kang AY, Zenker M, Ceremsak JJ, Stieglitz E, Muskens IS, Roberts W, McKean-Cowdin R, Metayer C, Roux PP, Wiemels JL. de Smith AJ, et al. Genes Chromosomes Cancer. 2019 Oct;58(10):723-730. doi: 10.1002/gcc.22765. Epub 2019 May 27. Genes Chromosomes Cancer. 2019. PMID: 31102422 Free PMC article.