首页 | 本学科首页   官方微博 | 高级检索  
     


Agenesis of the corpus callosum,developmental delay,autism spectrum disorder,facial dysmorphism,and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion
Authors:Ayeshah Chaudhry  Brian H. Chung  Dimitri J. Stavropoulos  Marcela P. Araya  Asim Ali  Elise Heon  David Chitayat
Affiliation:1. Department of Laboratory Medicine and Genetics, Trillium Health Partners, Mississauga, Ontario, Canada;2. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada;3. Department of Paediatric and Adolescent Medicine, University of Hong Kong, Hong Kong, Hong Kong;4. Department of Paediatric Laboratory Medicine, Division of Genome Diagnostics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada;5. Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada;6. Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada;7. Department of Obstetrics and Gynecology, The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada
Abstract:
Keywords:agenesis of corpus callosum (ACC)  array‐CGH  autism spectrum disorder  chromosome 10p11.22  corneal dystrophy  deletion  ZEB1
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号