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Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations.
Ovsyannikova GS, Fedorova DV, Tesakov IP, Martyanov AA, Ignatova AA, Ponomarenko EA, Zharkov PA, Pavlova AV, Raykina EV, Maschan MA, Panteleev MA, Novichkova GA, Sveshnikova AN, Smetanina NS. Ovsyannikova GS, et al. Among authors: maschan ma. Haematologica. 2022 Oct 1;107(10):2511-2516. doi: 10.3324/haematol.2022.281340. Haematologica. 2022. PMID: 35796010 Free PMC article. No abstract available.
Clinical and genomic heterogeneity of Diamond Blackfan anemia in the Russian Federation.
Smetanina NS, Mersiyanova IV, Kurnikova MA, Ovsyannikova GS, Hachatryan LA, Bobrynina VO, Maschan MA, Novichkova GA, Lipton JM, Maschan AA. Smetanina NS, et al. Among authors: maschan ma. Pediatr Blood Cancer. 2015 Sep;62(9):1597-600. doi: 10.1002/pbc.25534. Epub 2015 May 6. Pediatr Blood Cancer. 2015. PMID: 25946618 Free PMC article.