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Publications by Peter S Mortimer
Mutations in GATA2 Cause Primary Lymphedema Associated With a Predisposition to Acute Myeloid Leukemia (Emberger Syndrome)
Nature Genetics
Genetics
Physical Therapies for Reducing and Controlling Lymphoedema of the Limbs
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Acute Myeloid Leukemia With NPM1 Somatic Mutations
Nucleophosmin Mutations in Acute Myeloid Leukemia in Children
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Landscape of TET2 Mutations in Acute Myeloid Leukemia
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Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia
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Current Findings for Recurring Mutations in Acute Myeloid Leukemia
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RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)
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Myelodysplastic Syndrome, Juvenile Myelomonocytic Leukemia, and Acute Myeloid Leukemia Associated With Complete or Partial Monosomy 7
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Pattern Associated Leukemia Immunophenotypes and Measurable Disease Detection in Acute Myeloid Leukemia or Myelodysplastic Syndrome With Mutated NPM1
Cytometry Part B - Clinical Cytometry
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IDH1 and IDH2 Mutations in Therapy-Related Myelodysplastic Syndrome and Acute Myeloid Leukemia Are Associated With a Normal Karyotype and With Der(1;7)(q10;p10)
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