This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Almazni I, Stapley R, Morgan N, Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding, Front Cardiovasc Med. 2019; 6: 80.AlmazniIStapleyRMorganNInherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With BleedingFront Cardiovasc Med201968010.3389/fcvm.2019.00080659307331275945Search in Google Scholar
Luddy RE, Champion LA, Schwartz AD. A fatal myeloproliferative syndrome in a family with thrombocytopenia and platelet dysfunction. Cancer. 1978; 41: 1959-63.LuddyREChampionLASchwartzADA fatal myeloproliferative syndrome in a family with thrombocytopenia and platelet dysfunctionCancer19784119596310.1002/1097-0142(197805)41:5<1959::AID-CNCR2820410540>3.0.CO;2-8Search in Google Scholar
Galera P, Dulau-Florea A, Calvo KR. Inherited thrombocytopenia and platelet disorders with germline predisposition to myeloid neoplasia. Int J Lab Hematol. 2019; 41(Suppl. 1): 131– 141.GaleraPDulau-FloreaACalvoKRInherited thrombocytopenia and platelet disorders with germline predisposition to myeloid neoplasiaInt J Lab Hematol201941Suppl. 1131–14110.1111/ijlh.12999Search in Google Scholar
Luo X, Feurstein S, Mohan S, Porter CC, Jackson SA, Keel S, et al. ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants. Blood Adv. 2019 Oct 22; 3(20): 2962-2979.LuoXFeursteinSMohanSPorterCCJacksonSAKeelSet alClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variantsBlood Adv2019Oct 223202962297910.1182/bloodadvances.2019000644Search in Google Scholar
Tsai SC, Shih LY, Liang ST, Huang YJ, Kuo MC, Huang CF, et al. Biological Activities of RUNX1 Mutants Predict Secondary Acute Leukemia Transformation from Chronic Myelomonocytic Leukemia and Myelodysplastic Syndromes. Clin Cancer Res. 2015 Aug 1; 21(15): 3541-51.TsaiSCShihLYLiangSTHuangYJKuoMCHuangCFet alBiological Activities of RUNX1 Mutants Predict Secondary Acute Leukemia Transformation from Chronic Myelomonocytic Leukemia and Myelodysplastic SyndromesClin Cancer Res2015Aug 1211535415110.1158/1078-0432.CCR-14-2203Search in Google Scholar
Harada H, Harada Y, Niimi H, Kyo T, Kimura A, Inaba T. High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia. Blood. 2004 Mar 15; 103(6): 2316-24.HaradaHHaradaYNiimiHKyoTKimuraAInabaTHigh incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasiaBlood2004Mar 15103623162410.1182/blood-2003-09-3074Search in Google Scholar
Tang JL, Hou HA, Chen CY, Liu CY, Chou WC, Tseng MH, et al. AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations. Blood. 2009 Dec 17; 114(26): 5352-61.TangJLHouHAChenCYLiuCYChouWCTsengMHet alAML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterationsBlood2009Dec 171142653526110.1182/blood-2009-05-223784Search in Google Scholar
Deuitch N, Broadbridge E, Cunningham L, et al. RUNX1 Familial Platelet Disorder with Associated Myeloid Malignancies. 2021 Mar 4 [Updated 2021 May 6]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2022.DeuitchNBroadbridgeECunninghamLet alRUNX1 Familial Platelet Disorder with Associated Myeloid Malignancies2021Mar 4 [Updated 2021 May 6]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]Seattle (WA)University of Washington, Seattle1993-2022Search in Google Scholar