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Heterogeneous clinical presentation in icf syndrome: Correlation with underlying gene defects

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第一作者: Weemaes,C.M.
作者单位: Department of Pediatrics, University of North Carolina, Chapel Hill, NC, United States [1] Department of Pediatrics, Leiden University Medical Center, Leiden, Netherlands [2] Department of Pediatric Immunology and Allergy, Necmettin Erbakan University, Meram Medical Faculty [3] Laboratorio di Citogenetica, Instituto G Gaslini, Genova, Italy [4] Department of Pediatrics, Federico II University of Naples, Naples, Italy [5] Department of Paediatric Immunology, Newcastle Upon Tyne Hospital, Newcastle University, United [6] Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada [7] Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands [8] Department of Immunology, Erasmus Medical Center, Rotterdam, Netherlands [9] Department of Pediatrics, Haemato-Oncology Unit, Hopital Universitaire des Enfants Reine Fabiola [10] Department of Pediatric Immunology, Dr Sami Ulus Maternity and Children's, Research and Educational [11] Department of Immunohaematology and Blood Transfusion, Leiden University Medical Center, Leiden [12] Institute of Medical Molecular Genetics, University of Zurich, Zurich, Switzerland, Department of [13] Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands, Institutes of [14] Landesfrauen und Kinderklinik, Linz, Austria [15] Department of Pediatric Infectious Diseases and Immunology, Radboud University, Nijmegen Medical [16] Centre for Immunodeficiency, Great Ormond Street Hospital, Institute of Child Health, London [17] Department of Pediatrics and Adolescent Medicine, University Hospital Ulm, Ulm, Germany [18]
发布时间 2018-08-24
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European journal of human genetics: EJHG

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