Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at chromosome 18q22.1 and chromosome 13q12.3-q13.1.
作者信息
Bhatti D, Balasetti V, Malgireddy K, Rush E T, Torres-Russotto D
机构信息
Department of Neurological Sciences, University of Nebraska Medical Center, USA.
Department of Pediatrics, University of Nebraska Medical Center, USA; Department of Internal Medicine, University of Nebraska Medical Center, USA; Department of Orthopedic Surgery, University of Nebraska Medical Center, USA; Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center, USA.
出版信息
Parkinsonism Relat Disord. 2016 Nov;32:133-134. doi: 10.1016/j.parkreldis.2016.09.002. Epub 2016 Sep 4.
Abstract
摘要
Zotero 插件