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Plastic and reconstructive surgery, ISSN 0032-1052, 06/2018, Volume 141, Issue 6, pp. 1508 - 1516
Occurring once in every 2000 live births, craniosynostosis is one of the most frequent congenital anomalies encountered by the craniofacial surgeon. Syndromic... 
SURGERY | AUTISM | DE-NOVO MUTATIONS | AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS | CONGENITAL HEART-DISEASE | GROWTH-FACTOR RECEPTOR-2 | PFEIFFER-SYNDROME | CORONAL CRANIOSYNOSTOSIS | CROUZON-SYNDROME | SPECTRUM | SAGITTAL CRANIOSYNOSTOSIS
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 04/2017, Volume 54, Issue 4, pp. 260 - 268
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2014, Volume 9, Issue 7, p. e101693
Apert syndrome is an autosomal dominantly inherited disorder caused by missense mutations in fibroblast growth factor receptor 2 (FGFR2). Surgical procedures... 
FACTOR RECEPTOR-2 FGFR2 | APERT-SYNDROME | IMMUNE-RESPONSES | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | CALVARIAL BONE | CROUZON-SYNDROME | DIFFERENTIATION | SUSTAINED-RELEASE | GENE CAUSE | BONE-DEVELOPMENT | RNA-Binding Proteins - genetics | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Male | Acrocephalosyndactylia - genetics | Receptor, Fibroblast Growth Factor, Type 2 - administration & dosage | Drug Delivery Systems | Codon | Cranial Sutures - abnormalities | Fibroblast Growth Factor 2 - metabolism | Female | Acrocephalosyndactylia - therapy | Fibroblast Growth Factor 10 - genetics | Osteoblasts - cytology | Disease Models, Animal | Recombinant Proteins - metabolism | Cell Line | Gene Expression | Calcification, Physiologic - drug effects | Osteoblasts - drug effects | Mice, Transgenic | Recombinant Proteins - genetics | Polyethylene Glycols - administration & dosage | Recombinant Proteins - administration & dosage | Acrocephalosyndactylia - metabolism | Phenotype | Animals | Cell Differentiation - drug effects | Polyethyleneimine - administration & dosage | Protein Binding | Mice | Mutation | Osteoblasts - metabolism | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Amino Acid Substitution | Fibroblast growth factors | Genetic aspects | Health aspects | Analysis | Fibroblast growth factor | Phosphorylation | Animal models | Apert's syndrome | Craniosynostosis | Intracellular signalling | Genomes | Kinases | Osteoblasts | Proteins | Polymer chemistry | Biomedical materials | Missense mutation | Etiology | Mineralization | Rodents | Surgery | Sutures | Fibroblasts | Biocompatibility | Polymers | Growth factors | Fibroblast growth factor receptor 2 | Fibroblast growth factor 2 | Fibroblast growth factor 10 | Engineering schools | Dysostosis | Gene expression | Patients | Ligands | Apoptosis
Journal Article
American Journal of Medical Genetics Part c : Seminars in Medical Genetics, ISSN 1552-4868, 2013, Volume 163, Issue 4, pp. 259 - 270
Journal Article
Journal of Anatomy, ISSN 0021-8782, 07/2002, Volume 201, Issue 1, pp. 31 - 39
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2002, Volume 70, Issue 2, pp. 472 - 486
Journal Article