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Publications by Nameer Al Mardini
A New Family With a germlineANKRD26mutation and Predisposition to Myeloid Malignancies
Leukemia and Lymphoma
Cancer Research
Oncology
Hematology
Related publications
BAP1 Tumour Predisposition Syndrome: A New Mutation in One Family
Acta Dermato-Venereologica
Dermatology
Medicine
RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)
Seminars in Hematology
Hematology
Mutations in GATA2 Cause Primary Lymphedema Associated With a Predisposition to Acute Myeloid Leukemia (Emberger Syndrome)
Nature Genetics
Genetics
Clinical Spectrum and Clonal Evolution in Germline Syndromes With Predisposition to Myeloid Neoplasms
British Journal of Haematology
Hematology
ANKRD26-related Thrombocytopenia: Case Report and Literature Review of Inherited Thrombocytopenias With Predisposition to Malignancies
Pediatric Hematology/Oncology and Immunopathology
Oncology
Pediatrics
Child Health
Allergy
Hematology
Perinatology
Immunology
Managing Individuals With Propensity to Myeloid Malignancies Due to Germline RUNX1 Deficiency
Haematologica
Hematology
Community-Acquired Infections and Their Association With Myeloid Malignancies
Cancer Epidemiology
Cancer Research
Epidemiology
Oncology
How I Curate: Applying American Society of Hematology-Clinical Genome Resource Myeloid Malignancy Variant Curation Expert Panel Rules for RUNX1 Variant Curation for Germline Predisposition to Myeloid Malignancies
Haematologica
Hematology
Targeted Next-Generation Sequencing of Familial Platelet Disorder With Predisposition to Acute Myeloid Leukaemia
British Journal of Haematology
Hematology
