De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome (Q34388821)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome |
scientific article |
Statements
1 reference
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome (English)
1 reference
1 reference
M Oldridge
1 reference
E H Zackai
1 reference
D M McDonald-McGinn
1 reference
S Iseki
1 reference
G M Morriss-Kay
1 reference
S R Twigg
1 reference
D Johnson
1 reference
S A Wall
1 reference
E W Jabs
1 reference
1 February 1999
1 reference
1 reference
Identifiers
1 reference