Neuroimaging Findings in Patients with <i>EBF3</i> Mutations: Report of Two Cases.

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第一作者： Mar,Jiménez de la Peña

第一单位： Neuroimaging, Hospital Universitario Quirónsalud, Madrid, Spain.

作者： Mar,Jiménez de la Peña ^[1] ; Ana,Jiménez de Domingo ^[2] ; Pilar,Tirado ^[3] ; Beatriz,Calleja-Pérez ^[4] ; Luis A,Alcaraz ^[5] ; Sara,Álvarez ^[6] ; Jonathan,Williams ^[7] ; James R,Hagman ^[8] ; Andrea H,Németh ^[9] ; Alberto,Fernández-Jaén ^[10]

作者单位： Neuroimaging, Hospital Universitario Quirónsalud, Madrid, Spain. ^[1] Department of Pediatric Neurology, Hospital Universitario Quirónsalud, Madrid, Spain. ^[2] Department of Pediatric Neurology, Hospital Universitario La Paz, Madrid, Spain. ^[3] Pediatric Primary Care, C.S. Doctor Cirajas, Madrid, Spain. ^[4] Bioarray, Diagnóstico Genético, Alicante, Spain. ^[5] Genomics and Medicine, NIMGenetics, Madrid, Spain. ^[6] Oxford Medical Genetics Laboratories, Churchill Hospital, Oxford, United Kingdom. ^[7] Department of Immunology and Genomic Medicine, National Jewish Health, Denver, Colorado, USA. ^[8] Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom. ^[9] Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom. ^[10] Department of Pediatric Neurology, Hospital Universitario Quirónsalud, and Medicine School, Universidad Europea de Madrid, Madrid, Spain. ^[11]

关键词 ADHD Autism EBF3 Neuroimaging Tractography

DOI 10.1159/000513583

PMID 34177436

发布时间 2021-12-03

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Molecular syndromology

2021年12卷3期

186-193页

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Neuroimaging Findings in Patients with <i>EBF3</i> Mutations: Report of Two Cases.

Molecular syndromology

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Neuroimaging Findings in Patients with <i>EBF3</i> Mutations: Report of Two Cases.

Molecular syndromology

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Molecular syndromology

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