Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome)

✍ Scribed by Sarasua, S. M.; Dwivedi, A.; Boccuto, L.; Rollins, J. D.; Chen, C.-F.; Rogers, R. C.; Phelan, K.; DuPont, B. R.; Collins, J. S.

• Book ID: 125473685
• Publisher: BMJ Publishing Group
• Year: 2011
• Tongue: English
• Weight: 235 KB
• Volume: 48
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmedgenet-2011-100225