|
YAMAMOTO Toshiyuki
Department School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine Position Professor |
|
| Article types | Case report |
| Language | English |
| Peer review | Peer reviewed |
| Title | Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosis. |
| Journal | Formal name：European Journal of Medical Genetics Abbreviation：Eur J Med Genet ISSN code：17697212 |
| Domestic / Foregin | Foregin |
| Volume, Issue, Page | 59(11),pp.559-563 |
| Author and coauthor | Shimojima K, Ondo Y, Matsufuji M, Sano N, Tsuru H, Oyoshi T, Higa N, Tokimura H, Arita K, Yamamoto T. |
| Authorship | Last author,Corresponding author |
| Publication date | 2016/10 |
| DOI | 10.1016/j.ejmg.2016.10.006 |