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Publications by Colin G Steward

Mutations in GATA2 Cause Primary Lymphedema Associated With a Predisposition to Acute Myeloid Leukemia (Emberger Syndrome)

Nature Genetics

Genetics

2011

English

Diagnosing Haemophagocytic Syndrome

Archives of Disease in Childhood

English

Related publications

Acute Myeloid Leukemia With NPM1 Somatic Mutations

2020

English

Nucleophosmin Mutations in Acute Myeloid Leukemia in Children

English

Landscape of TET2 Mutations in Acute Myeloid Leukemia

English

Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia

Stem Cell Reports

Biochemistry

Genetics

Developmental Biology

Cell Biology

2019

English

Current Findings for Recurring Mutations in Acute Myeloid Leukemia

Journal of Hematology and Oncology

English

RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)

Seminars in Hematology

Hematology

2017

English

Myelodysplastic Syndrome, Juvenile Myelomonocytic Leukemia, and Acute Myeloid Leukemia Associated With Complete or Partial Monosomy 7

English

Pattern Associated Leukemia Immunophenotypes and Measurable Disease Detection in Acute Myeloid Leukemia or Myelodysplastic Syndrome With Mutated NPM1

Cytometry Part B - Clinical Cytometry

English

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)

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Colin G Steward

Mutations in GATA2 Cause Primary Lymphedema Associated With a Predisposition to Acute Myeloid Leukemia (Emberger Syndrome)

Diagnosing Haemophagocytic Syndrome

Related publications

Acute Myeloid Leukemia With NPM1 Somatic Mutations

Nucleophosmin Mutations in Acute Myeloid Leukemia in Children

Landscape of TET2 Mutations in Acute Myeloid Leukemia

Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia

Current Findings for Recurring Mutations in Acute Myeloid Leukemia

RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)

Myelodysplastic Syndrome, Juvenile Myelomonocytic Leukemia, and Acute Myeloid Leukemia Associated With Complete or Partial Monosomy 7

Pattern Associated Leukemia Immunophenotypes and Measurable Disease Detection in Acute Myeloid Leukemia or Myelodysplastic Syndrome With Mutated NPM1

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)