首页 | 本学科首页   官方微博 | 高级检索  
     


Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literature
Authors:Laura Travan  Samuele Naviglio  Angela De Cunto  Andrea Pellegrin  Vanna Pecile  Alessandro Mauro Spinelli  Stefania Cappellani  Flavio Faletra
Affiliation:1. Department of Perinatal Medicine, Institute for Maternal and Child Health IRCCS Burlo Garofolo, Trieste, Italy;2. Department of Medicine, Surgery, and Health Sciences, University of Trieste, Trieste, Italy;3. Department of Pediatric Radiology, Institute for Maternal and Child Health IRCCS Burlo Garofolo, Trieste, Italy;4. Department of Genetics, Institute for Maternal and Child Health IRCCS Burlo Garofolo, Trieste, Italy;5. University of Padua, Padua, Italy
Abstract:
Keywords:19q13.32  copy number variation  developmental delay  microdeletion  SNPs array
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