Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily (Q46869444)
Jump to navigation
Jump to search
scientific article published in February 2009
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily |
scientific article published in February 2009 |
Statements
1 reference
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily (English)
1 reference
1 reference
1 reference
Tony Roscioli
1 reference
Dale J Hedges
1 reference
Indira B Taylor
1 reference
David Johnson
1 reference
David J David
1 reference
1 February 2009
1 reference
1 reference
30
1 reference
2
1 reference
204-211
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference