TY  - GEN
AU  - Reardon,W
AU  - Wilkes,D
AU  - Rutland,P
AU  - Pulleyn,L J
AU  - Malcolm,S
AU  - Dean,J C
AU  - Evans,R D
AU  - Jones,B M
AU  - Hayward,R
AU  - Hall,C M
AU  - Nevin,N C
AU  - Baraister,M
AU  - Winter,R M
TI  - Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis
SN  - 0022-2593
PY  - 1997///1006
KW  - Acrocephalosyndactylia
KW  - genetics
KW  - Adult
KW  - Arginine
KW  - Child
KW  - Child, Preschool
KW  - Craniosynostoses
KW  - Female
KW  - Fibroblast Growth Factors
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Mutation
KW  - Proline
KW  - Protein-Tyrosine Kinases
KW  - Receptor, Fibroblast Growth Factor, Type 3
KW  - Receptors, Fibroblast Growth Factor
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmg.34.8.632
ER  -