Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes

Fotios Asimakopoulos; Sir Nicholas White; Tracey Holloway; Elisabeth P. Nacheva; Anthony R. Green

doi:10.1016/0145-2126(94)90218-6

Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes

Leukemia Research 18: 43-43

Article 1994 French

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Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes

Abstract

Discussion(0)

Related publications

Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes

The human <i>CD40</i> gene lies within chromosome 20q deletions associated with myeloid malignancies

32 ACTIVATION OF REDOX-SENSITIVE INFLAMMASOMES UNDERLIES THE BIOLOGICAL PHENOTYPE OF MYELODYSPLASTIC SYNDROMES

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Polymorphism in exon 6 of the dopamine D2 receptor gene (DRD2) is associated with elevated blood pressure and personality disorders in men