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Craniosynostosis
Benjamin S. Carson
School of Medicine
Research output
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Chapter in Book/Report/Conference proceeding
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Keyphrases
Apert
33%
Cerebral Atrophy
33%
Clinical Features
33%
Craniosynostosis
100%
Crouzon Syndrome
33%
Fibroblast Growth Factor Receptor 1 (FGFR1)
66%
Genetic Influences
33%
Mechanical Influence
33%
Metopic
33%
Nonsyndromic
33%
Pathophysiology
33%
Premature Fusion
33%
Receptor Gene
66%
Sagittal
33%
Single Suture
66%
Specific mutation
33%
Syndromic
33%
Weiss
33%
Medicine and Dentistry
Cerebral Atrophy
25%
Clinical Feature
25%
Craniofacial Synostosis
100%
Crouzon Syndrome
25%
Fibroblast Growth Factor Receptor
50%
Pathophysiology
25%
Prematurity
25%
Receptor Gene
50%
Suture Material
100%
Pharmacology, Toxicology and Pharmaceutical Science
Brain Atrophy
33%
Clinical Feature
33%
Craniofacial Synostosis
100%
Crouzon Syndrome
33%
Fibroblast Growth Factor Receptor
66%
Pathophysiology
33%
Prematurity
33%
Biochemistry, Genetics and Molecular Biology
Fibroblast Growth Factor Receptor
100%
Genetics
50%
Receptor Gene
100%
Neuroscience
Fibroblast Growth Factor Receptor
100%
Receptor Gene
100%