Articles

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations

National Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK;Wellcome Trust Centre for Human Genetics, University of Oxford, UK
Nuffield Department of Medicine, University of Oxford, UK
Hematology Department, Centro Hospitalar e Universitário de Coimbra, Portugal
Department of Pediatrics and Adolescent Medicine, University Medical Center, Ulm, Germany
National Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK;Wellcome Trust Centre for Human Genetics, University of Oxford, UK
Centre for Cancer Research and Cell Biology, Queen’s University, Belfast, UK
Department of Clinical Chemistry and Hematology, University Medical Center Utrecht, the Netherlands;A list of members and affiliations is provided in the Online Supplementary Information
Nuffield Department of Medicine, University of Oxford, UK
Department of Physiology, Anatomy and Genetics, University of Oxford, UK
National Institute for Health Research (NIHR) Comprehensive Biomedical Research Centre, Oxford, UK;Wellcome Trust Centre for Human Genetics, University of Oxford, UK
Vol. 101 No. 11 (2016): November, 2016 https://doi.org/10.3324/haematol.2016.144063