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Publications by David J. Rabbolini
The Clinical Heterogeneity of RUNX1 Associated Familial Platelet Disorder With Predisposition to Myeloid Malignancy - A Case Series and Review of the Literature
Research and Practice in Thrombosis and Haemostasis
DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-Generation Sequencing Technology With a Candidate Gene Array
Related publications
RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)
Seminars in Hematology
Hematology
Targeted Next-Generation Sequencing of Familial Platelet Disorder With Predisposition to Acute Myeloid Leukaemia
British Journal of Haematology
Hematology
Hepatocelluar Carcinoma Associated With Attenuated Familial Adenomatous Polyposis: A Case Report and Review of the Literature
Clinical Colorectal Cancer
Oncology
Gastroenterology
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
Familial Chordoma: A Case Report and Review of the Literature
Oncology Letters
Cancer Research
Oncology
Autism Spectrum Disorder Associated With 49,XYYYY: Case Report and Review of the Literature
BMC Medical Genetics
Genetics
Chordoma: A Case Series and Review of the Literature
Journal of Medical Case Reports
Medicine
Is There a Thrombotic Tendency in Patients With Familial Mediterranean Fever? A Small Case Series and Review of the Literature
Annals of Paediatric Rheumatology
Clinical Characteristics of Hereditary Hemorrhagic Telangiectasia - Case Series and Review of the Literature
Vojnosanitetski Pregled
Medicine
Pharmacology
