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Two novel RUNX1 mutations in a patient with congenital thrombocytopenia that evolved into a high grade myelodysplastic syndrome.
Schmit, Jessica M; Turner, Daniel J; Hromas, Robert A; Wingard, John R; Brown, Randy A; Li, Ying; Li, Marilyn M; Slayton, William B; Cogle, Christopher R.
Affiliation
  • Schmit JM; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Turner DJ; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Hromas RA; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Wingard JR; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Brown RA; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Li Y; Division of Hematopathology, Department of Pathology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Li MM; Cancer Genetics Laboratory, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Slayton WB; Division of Hematology and Oncology, Department of Pediatrics, College of Medicine, University of Florida, Gainesville, FL, USA.
  • Cogle CR; Division of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
Leuk Res Rep ; 4(1): 24-7, 2015.
Article in En | MEDLINE | ID: mdl-25893166

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Leuk Res Rep Year: 2015 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Leuk Res Rep Year: 2015 Document type: Article Affiliation country: Estados Unidos