Keyphrases
Fibroblast Growth Factor Receptor 3 (FGFR3)
100%
Achondroplasia
100%
Thanatophoric Dysplasia
100%
Dwarfism
42%
Endochondral Ossification
14%
Cell Proliferation
14%
Autosomal Dominant
14%
Receptor Tyrosine Kinase
14%
Gene mutation
14%
Skeletal Disorders
14%
Extracellular Domain
14%
Transmembrane Domain
14%
Tyrosine Phosphorylation
14%
Missense mutation
14%
Long Bone
14%
Ligand-independent
14%
Neonatal Lethality
14%
Tyrosine Kinase Domain
14%
Non-lethal
14%
Longitudinal Growth
14%
Continuous Process
14%
Hypochondroplasia
14%
Biochemistry, Genetics and Molecular Biology
Dysplasia
100%
Fibroblast Growth Factor Receptor 3
100%
Endochondral Ossification
16%
Autosomal Dominant Inheritance
16%
Receptor Tyrosine Kinase
16%
Tyrosine Kinase
16%
Gene Mutation
16%
Cell Proliferation
16%
Tyrosine Phosphorylation
16%
Transmembrane Domain
16%
Missense Mutation
16%
Continuous Process
16%