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Blood, ISSN 0006-4971, 02/2014, Volume 123, Issue 6, pp. 809 - 821
Journal Article
Best Practice & Research: Clinical Haematology, ISSN 1521-6926, 2014, Volume 28, Issue 1, pp. 55 - 68
Myelodysplastic syndromes (MDS) are clonal hematopoietic disorders characterized by cytopenias, ineffective hematopoiesis, myelodysplasia, and an increased... 
Hematology, Oncology and Palliative Medicine | familial MDS | CEBPA | Shwachman-Diamond Syndrome | Diamond-Blackfan Anemia | Severe Congenital Neutropenia | MonoMac | FPD/AML | Fanconi Anemia | familial leukemia | GATA2 | Dyskeratosis Congenita | RUNX1 | SRP72 | bone marrow failure syndromes | Emberger Syndrome | myelodysplastic syndromes | genetic predisposition | MDS | Congenital Amegakaryocytic Thrombocytopenia | Thrombocytopenia | Congenital Amegakaryocytic | genetic predisposition familial | Keywords myelodysplastic syndromes | FAMILIAL PLATELET DISORDER | BLACKFAN ANEMIA | G-CSF THERAPY | DYSKERATOSIS-CONGENITA | HEMATOLOGY | ACUTE MYELOID-LEUKEMIA | SHWACHMAN-DIAMOND-SYNDROME | FANCONI-ANEMIA | AUTOSOMAL-DOMINANT | Genetic Predisposition to Disease | Leukemia, Myeloid, Acute - pathology | Humans | Signal Recognition Particle - genetics | Hematopoietic Stem Cell Transplantation | Antineoplastic Agents - therapeutic use | Dyskeratosis Congenita - genetics | Myelodysplastic Syndromes - diagnosis | Myelodysplastic Syndromes - therapy | Fanconi Anemia - diagnosis | Leukemia, Myeloid, Acute - diagnosis | Dyskeratosis Congenita - diagnosis | Adolescent | Dyskeratosis Congenita - pathology | Fanconi Anemia - pathology | Aged | Fanconi Anemia - genetics | Myelodysplastic Syndromes - genetics | CCAAT-Enhancer-Binding Proteins - genetics | Mutation | Myelodysplastic Syndromes - pathology | Core Binding Factor Alpha 2 Subunit - genetics | GATA2 Transcription Factor - genetics | Leukemia, Myeloid, Acute - genetics | Leukemia | Fanconi's anemia | AML | Myelodysplastic syndromes | FPD
Journal Article
Journal Article
Blood, ISSN 0006-4971, 02/2014, Volume 123, Issue 6, pp. 863 - 874
Journal Article
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 71 - 71
Journal Article
Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 2017, Volume 5, Issue 4, pp. 1149 - 1152.e1
Initial sequencing of the GATA2 gene was performed by Sanger methodology and no mutation was identified. Because of high clinical suspicion for GATA2... 
Internal Medicine | Allergy and Immunology | ALLERGY | PRIMARY LYMPHEDEMA | CELL-MEDIATED-IMMUNITY | DISEASE | DYSPLASIA | MUTATIONS | IMMUNOLOGY | MONOMAC SYNDROME | Dendritic cells | Laboratories | Cytotoxicity | Infections | Gene deletion | Patients | Hemopoiesis | Human papillomavirus | Lymphedema | Clonal deletion | Lymphocytes | Biopsy | Mutation | Viral infections
Journal Article
Journal Article