Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily
(Q46869444)
scientific article published in February 2009
scientific article published in February 2009
Language:
Current Data About
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily
other details
| description | scientific article published in February 2009 |
External Links
| (P356) |
10.1002/HUMU.20825
|
| (P698) |
18726952
|
| (P8608) |
release_grnpzh7msfbplpigv55rlymlya
|