Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: Clinical spectrum, prevalence, and surgical outcome

Journal of Neurosurgery

Volumn 92, Issue 4, 2000, Pages 631-636

  Renier, Dominique ^a   Ghouzzi, Vincent El ^a   Bonaventure, Jacky ^a   Merrer, Martine Le ^a   Lajeunie, Elizabeth ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Brachycephaly; Children; Craniosynostosis; Fibroblast growth factor receptor 3 mutation; Plagiocephaly

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ARTICLE; BRACHYCEPHALY; BRACHYDACTYLY; CRANIOFACIAL SYNOSTOSIS; FEMALE; GENE MUTATION; HUMAN; HYPERTELORISM; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; TEMPORAL BONE;

EID: 0034069610     PISSN: 00223085     EISSN: None     Source Type: Journal    
DOI: 10.3171/jns.2000.92.4.0631     Document Type: Article

References (17)

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