TY  - GEN
AU  - Pulleyn,L J
AU  - Reardon,W
AU  - Wilkes,D
AU  - Rutland,P
AU  - Jones,B M
AU  - Hayward,R
AU  - Hall,C M
AU  - Brueton,L
AU  - Chun,N
AU  - Lammer,E
AU  - Malcolm,S
AU  - Winter,R M
TI  - Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus
SN  - 1018-4813
PY  - 1997///0304
KW  - Craniosynostoses
KW  - diagnostic imaging
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Male
KW  - Pedigree
KW  - Phenotype
KW  - Point Mutation
KW  - Radiography
KW  - Receptor Protein-Tyrosine Kinases
KW  - genetics
KW  - Receptor, Fibroblast Growth Factor, Type 2
KW  - Receptors, Fibroblast Growth Factor
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1159/000472215
ER  -