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PedAM

Pediatric Disease Annotations & Medicines




Disease thrombocytosis
Phenotype C0023467|acute myeloid leukemia
Sentences 2
PubMedID- 25932448 A novel case of extreme thrombocytosis in acute myeloid leukemia associated with isochromosome 17q and copy neutral loss of heterozygosity.
PubMedID- 22579367 A novel prognosis of acute myeloid leukemia: aml-m2 complicate with thrombocythemia after complete remission.

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