Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Fiona C Connell

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

Nature Genetics
Genetics
2011English

Related publications

Acute Myeloid Leukemia With NPM1 Somatic Mutations

2020English

Nucleophosmin Mutations in Acute Myeloid Leukemia in Children

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
2007English

Landscape of TET2 Mutations in Acute Myeloid Leukemia

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
2011English

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

Stem Cell Reports
BiochemistryGeneticsDevelopmental BiologyCell Biology
2019English

Current Findings for Recurring Mutations in Acute Myeloid Leukemia

Journal of Hematology and Oncology
Cancer ResearchOncologyHematologyMolecular Biology
2011English

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

Seminars in Hematology
Hematology
2017English

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

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
1999English

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

Cytometry Part B - Clinical Cytometry
Forensic MedicinePathologyHistologyCell Biology
2018English

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)

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
2012English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy