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Blood, ISSN 0006-4971, 2009, Volume 114, Issue 5, pp. 937 - 951
Recently the World Health Organization (WHO), in collaboration with the European Association for Haematopathology and the Society for Hematopathology,... 
ACUTE UNDIFFERENTIATED LEUKEMIA | BALANCED CHROMOSOME-ABERRATIONS | TRANSIENT MYELOPROLIFERATIVE DISORDER | ACUTE LYMPHOBLASTIC-LEUKEMIA | ACUTE BIPHENOTYPIC LEUKEMIA | TYROSINE KINASE JAK2 | MYELODYSPLASTIC SYNDROMES MDS | HEMATOLOGY | INDEPENDENT PROGNOSTIC RELEVANCE | CHRONIC MYELOMONOCYTIC LEUKEMIA | ACQUIRED APLASTIC-ANEMIA | Leukemia - pathology | Cell Count | Humans | Myelodysplastic Syndromes - classification | Myeloproliferative Disorders - pathology | Myelodysplastic-Myeloproliferative Diseases - pathology | Myeloproliferative Disorders - genetics | Leukemia - classification | Neoplastic Stem Cells - pathology | Leukemia - genetics | Myeloproliferative Disorders - diagnosis | Acute Disease | Mastocytosis, Systemic - classification | World Health Organization | Myeloproliferative Disorders - classification | Terminology as Topic | Bone Marrow Examination - standards | Myelodysplastic-Myeloproliferative Diseases - genetics | Hematologic Neoplasms - classification | Cell Lineage | Myelodysplastic Syndromes - diagnosis | Myelodysplastic-Myeloproliferative Diseases - diagnosis | Eosinophilia - classification | Chromosome Aberrations | Leukemia - diagnosis | Myelodysplastic Syndromes - genetics | Mutation | Myelodysplastic Syndromes - pathology | Myelodysplastic-Myeloproliferative Diseases - classification | Preleukemia - classification
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2016, Volume 48, Issue 7, pp. 792 - 797
Journal Article
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2013, Volume 110, Issue 42, pp. E4016 - E4025
Journal Article
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 02/2015, Volume 125, Issue 2, pp. 563 - 570
Mutations in the essential telomerase genes TERT and TR cause familial pulmonary fibrosis; however, in telomerase-null mice, short telomeres predispose to... 
MEDICINE, RESEARCH & EXPERIMENTAL | REVERSE-TRANSCRIPTASE | DISEASE | TETRAHYMENA | RISK | TERMINAL TRANSFERASE | PHENOTYPES | IDIOPATHIC PULMONARY-FIBROSIS | APLASTIC-ANEMIA | COPD | PROCESSIVITY | Chromosome Disorders - epidemiology | Prevalence | Pneumothorax - enzymology | Humans | Middle Aged | Male | Pulmonary Fibrosis - genetics | Pulmonary Fibrosis - epidemiology | Incidence | Telomerase - genetics | Chromosome Disorders - enzymology | Pulmonary Emphysema - genetics | Adult | Female | Registries | Telomerase - metabolism | Telomere - genetics | Chromosome Disorders - pathology | alpha 1-Antitrypsin - genetics | Pneumothorax - epidemiology | Pulmonary Emphysema - pathology | Smoking - genetics | Pulmonary Fibrosis - pathology | Sex Characteristics | Smoking - metabolism | Pneumothorax - pathology | Telomere - pathology | Animals | Smoking - epidemiology | Pulmonary Fibrosis - enzymology | Telomere - enzymology | Sex Factors | Smoking - pathology | Mice | Pneumothorax - genetics | alpha 1-Antitrypsin - metabolism | Mutation | Pulmonary Emphysema - epidemiology | Chromosome Disorders - genetics | Pulmonary Emphysema - enzymology | Smokers | Gene mutations | Emphysema, Pulmonary | Genetic aspects | Telomerase | Identification and classification | Health aspects | Risk factors | Enzymes | Liver diseases | Pulmonary fibrosis | Cloning | Cell division | Chronic obstructive pulmonary disease | Emphysema | Deoxyribonucleic acid--DNA
Journal Article