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life sciences & biomedicine (19) 19
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BMC medical genetics, ISSN 1471-2350, 04/2019, Volume 20, Issue 1, pp. 64 - 64
.... Patients with GATA2 mutation have a high risk of developing myelodysplastic syndrome or acute myeloid... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Male | Mycobacterium Infections, Nontuberculous - complications | Anti-Bacterial Agents - therapeutic use | GATA2 Deficiency - genetics | Mycobacterium Infections, Nontuberculous - microbiology | Adult | Mycobacterium kansasii - isolation & purification | Myelodysplastic Syndromes - genetics | Mutation | Mycobacterium Infections, Nontuberculous - genetics | GATA2 Transcription Factor - genetics | Mycobacterium Infections, Nontuberculous - drug therapy | Care and treatment | Transcription factors | Gene mutations | Analysis | Mycobacterial infections | Immunological deficiency syndromes | Genetic aspects | Diagnosis | Health aspects | Risk factors | Myelodysplastic syndromes | Anemia | Leukemia | Antifungal agents | Immunodeficiency | Transplantation | Genetic transcription | Hypothyroidism | Hematopoietic stem cells | Virus diseases | Infection | Thyroid hormones | Refractory anemia | Transplants & implants | Stem cell transplantation | Cardiovascular disease | Infections | Thyroid gland | Myelodysplasia | Arthritis | Blood | Myelodysplastic syndrome | Genetic screening | Genetic disorders | Bacterial infections | Myeloid leukemia | Gene expression | Patients | Hemopoiesis | Chemotherapy | Tuberculosis | Pancytopenia | Stem cells | Skin | Acute myeloid leukemia | Tumors | Index Medicus | GATA-2 mutation | Mycobacterium kansasii | MonoMAC syndrome
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 risk of acute myeloid leukemia (AML... 
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 | Life Sciences & Biomedicine | Hematology | Science & Technology | 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 | Index Medicus | AML | Myelodysplastic syndromes | FPD
Journal Article
Leukemia & lymphoma, ISSN 1042-8194, 07/2019, Volume 60, Issue 8, pp. 2025 - 2033
Germline mutations in GATA2 are associated with a complex immunodeficiency and cancer predisposition syndrome... 
immunodeficiency | Emberger syndrome | GATA2 | pulmonary alveolar proteinosis | MonoMAC syndrome | Oncology | Life Sciences & Biomedicine | Hematology | Science & Technology | Index Medicus
Journal Article
Journal of leukocyte biology, ISSN 0741-5400, 06/2016, Volume 99, Issue 6, pp. 1065 - 1076
GATA2 deficiency formerly described as MonoMAC syndrome; dendritic cells, monocytes, B cells, and natural killer cell deficiency... 
Life Sciences | Human health and pathology | Tissues and Organs
Journal Article
Seminars in hematology, ISSN 0037-1963, 04/2017, Volume 54, Issue 2, pp. 81 - 86
Journal Article
Journal Article