Coexistence of JAK2V617F mutation and isolated del(5q) in a patient with thrombocytosis
Med Clin (Barc). 2021 Jun 25;156(12):625-627.
doi: 10.1016/j.medcli.2020.04.065.
Epub 2020 Aug 7.
[Article in
English,
Spanish]
Affiliations
- 1 ICO Badalona-Hospital Germans Trias i Pujol, Institut de Recerca contra la Leucèmia Josep Carreras, UAB, Badalona, Spain. Electronic address: smarce@iconcologia.net.
- 2 ICO Badalona-Hospital Germans Trias i Pujol, Institut de Recerca contra la Leucèmia Josep Carreras, UAB, Badalona, Spain.
- 3 Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar and GRETNHE, Cancer Research Program, IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
No abstract available
MeSH terms
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Chromosome Deletion
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Humans
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Mutation
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Myelodysplastic Syndromes* / genetics
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Thrombocytosis* / genetics