机译:2Q23.1的互惠删除和重复表明了MBD5在自闭症谱系障碍中的作用
Department of Human and Molecular Genetics Virginia Commonwealth University School of Medicine;
Signature Genomic Laboratories PerkinElmer Inc. Spokane WA United States;
Service of Genetics and Prenatal Diagnosis University and Polytechnic Hospital la Fe Valencia;
Department of Human Genetics Radboud University Nijmegen Medical Center Nijmegen Netherlands;
Department of Human Genetics University of Chicago Chicago IL United States;
Department of Pathology and Laboratory Medicine Nationwide Children's Hospital Columbus OH;
Department of Pediatrics McMaster University Medical Center McMaster Children's Hospital;
Department of Pediatrics McMaster University Medical Center McMaster Children's Hospital;
Division of Clinical and Metabolic Genetics Hospital for Sick Children University of Toronto;
Service of Genetics and Prenatal Diagnosis University and Polytechnic Hospital la Fe Valencia;
GeneDx Gaithersburg MD United States;
Cytogenetics Laboratory Department of Pediatric Laboratory Medicine Hospital for Sick Children;
Department of Pediatrics Nationwide Children's Hospital Columbus OH United States;
Department of Laboratory Medicine and Pathology Mayo Clinic Rochester MN United States;
Department of Laboratory Medicine and Pathology Mayo Clinic Rochester MN United States;
Center for Human Genetic Research Massachusetts General Hospital Boston MA United States;
Center for Human Genetic Research Massachusetts General Hospital Boston MA United States;
Department of Molecular and Medical Genetics Child Development and Rehabilitation Center Oregon;
Department of Molecular and Medical Genetics Child Development and Rehabilitation Center Oregon;
Laboratory Corporation of America Research Triangle Park Durham NC United States;
Department of Pathology and Laboratory Medicine Nationwide Children's Hospital Columbus OH;
Department of Human Genetics University of Chicago Chicago IL United States;
Paw Print Genetics Genetic Veterinary Sciences Inc. Spokane WA United States;
Center for Human Genetic Research Massachusetts General Hospital Boston MA United States;
Department of Human Genetics Radboud University Nijmegen Medical Center Nijmegen Netherlands;
Division of Clinical and Metabolic Genetics Hospital for Sick Children University of Toronto;
Department of Human and Molecular Genetics Virginia Commonwealth University School of Medicine;
2q23.1; autism spectrum disorder; gene dosage; MBD5; microdeletion; microduplication;
机译:在2q23.1的相互删除和重复表明MBD5在自闭症谱系障碍中的作用
机译:对2q23.1微缺失综合症的评估表明MBD5是智力残疾,癫痫和自闭症谱系障碍的单一病因源。
机译:基因组拷贝数变异分析暗示了中国婴儿痉挛症儿童的MBD5和HNRNPU基因,并扩大了2q23.1缺失的临床范围
机译:音乐疗法在促进自闭症谱系障碍儿童的沟通和社会技能方面的作用:试点研究
机译:时间加工和神经发育障碍:从注意力缺陷/多动障碍,自闭症谱系障碍和22q11.2删除综合征的见解。
机译:在2q23.1的相互删除和重复表明MBD5在自闭症谱系障碍中的作用
机译:2q23.1微缺失综合征的评估表明MBD5是智力残疾,癫痫症和自闭症谱系障碍的单一病因源