Deletion of 5q31 is observed in megakaryocytic cells in patients with myelodysplastic syndromes and a del(5q), including the 5q- syndrome
✍ Scribed by Catherine Godon; Pascaline Talmant; Richard Garand; Françoise Accart; Régis Bataille; Hervé Avet-Loiseau
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 53 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Autoimmune-thrombocytopenia was the striking feature in a patient with typical clinical symptoms of systemic lupus erythematosus (SLE), complement C4 deficiency, and positive lupus serology. However, myelodysplasia was found in the bone marrow and chromosome analysis revealed a deletion of the long
We identified a novel human long fatty acyl CoA synthetase 2 gene, ACS2, as a new ETV6 fusion partner gene in a recurrent t(5;12)(q31;p13) translocation in a patient with refractory anemia with excess blasts (RAEB) with basophilia, a patient with acute myelogenous leukemia (AML) with eosinophilia, a