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British Journal of Haematology, ISSN 0007-1048, 08/2014, Volume 166, Issue 4, pp. 550 - 556
Journal Article
Nature Medicine, ISSN 1078-8956, 02/2010, Volume 16, Issue 2, pp. 198 - 204
Journal Article
Journal Article
Atlas of Genetics and Cytogenetics in Oncology and Haematology, ISSN 1768-3262, 2018, Volume 22, Issue 7, pp. 298 - 302
Journal Article
Leukemia, ISSN 0887-6924, 09/2013, Volume 27, Issue 9, pp. 1852 - 1860
Chronic myeloid malignancies are categorized to the three main categories myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDSs) and MDS/MPN... 
monosomy 7 | MDS/MPN | SETBP1 | aCML | i(q10) | molecular marker | POLYCYTHEMIA-VERA | ACUTE MYELOID-LEUKEMIA | ESSENTIAL THROMBOCYTHEMIA | MOLECULAR MUTATIONS | ACTIVATING MUTATION | ONCOLOGY | CHRONIC MYELOPROLIFERATIVE DISORDERS | EXON 12 MUTATIONS | JAK2 | HEMATOLOGY | MYELODYSPLASTIC SYNDROMES | CHRONIC MYELOMONOCYTIC LEUKEMIA | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - diagnosis | Humans | Middle Aged | Male | Isochromosomes | Young Adult | Aged, 80 and over | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - genetics | Adult | Female | Nuclear Proteins - genetics | Chromosome Deletion | Proto-Oncogene Proteins c-cbl - genetics | Repressor Proteins - genetics | Mutation Rate | Myelodysplastic-Myeloproliferative Diseases - genetics | Chromosomes, Human, Pair 7 | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - mortality | Carrier Proteins - genetics | Myelodysplastic-Myeloproliferative Diseases - mortality | Myelodysplastic Syndromes - diagnosis | Myelodysplastic-Myeloproliferative Diseases - diagnosis | Bone Marrow - pathology | Myelodysplastic Syndromes - mortality | Aged | Myelodysplastic Syndromes - genetics | Mutation | Gene mutations | Physiological aspects | Genetic aspects | Research | Binding proteins | Myelodysplastic syndromes | Risk factors | Myeloproliferative disorders
Journal Article
Hematology/Oncology Clinics of North America, ISSN 0889-8588, 08/2018, Volume 32, Issue 4, pp. 729 - 743
Myelodysplastic syndromes (MDS) in children and adolescents are a rare heterogeneous group of clonal stem cell disorders. Complete or partial loss of... 
Pediatric MDS | SAMD9L | SAMD9 | GATA2 | Monosomy 7 | METHYLTRANSFERASE GENE EZH2 | CLONAL EVOLUTION | ACUTE MYELOID-LEUKEMIA | SAMD9L MUTATIONS CAUSE | WORLD-HEALTH-ORGANIZATION | SOMATIC MUTATIONS | ONCOLOGY | GATA2 DEFICIENCY | RETROSPECTIVE ANALYSIS | HEMATOLOGY | APLASTIC-ANEMIA | BONE-MARROW FAILURE
Journal Article
Journal Article
Journal Article
Journal of pediatric hematology/oncology, ISSN 1077-4114, 04/2019, Volume 41, Issue 3, pp. e177 - e178
Monosomy 7 may be a poor prognostic indicator in pediatric myelodysplastic syndrome. There are case reports of children with monosomy 7 who undergo spontaneous... 
monosomy 7 | acute myeloid leukemia | spontaneous remission | ONCOLOGY | PEDIATRICS | pediatric myelodysplastic syndrome | MUTATIONS | HEMATOLOGY | MYELODYSPLASTIC SYNDROME | CHILDREN | Dosage and administration | Diagnosis | Research | Drug therapy | Pediatric research | Immunosuppressive agents | Monosomy
Journal Article
Blood, ISSN 0006-4971, 06/2007, Volume 109, Issue 11, pp. 4641 - 4647
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 07/2019, Volume 96, Issue 4, pp. 300 - 309
Journal Article