Prominent basal emissary foramina in syndromic craniosynostosis: Correlation with phenotypic and molecular diagnoses

American Journal of Neuroradiology

Volumn 21, Issue 9, 2000, Pages 1707-1717

  Robson, C D ^a   Mulliken, J B ^a   Robertson, R L ^a   Proctor, M R ^a   Steinberger, D ^a   Barnes, P D ^a   McFarren, A ^a   Muller, U ^a   Zurakowski, D ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ACANTHOSIS NIGRICANS; ACROCEPHALOSYNDACTYLY; ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; DIAGNOSTIC ACCURACY; DISEASE CLASSIFICATION; FEMALE; GENE MUTATION; HUMAN; INFANT; INFECTIOUS MONONUCLEOSIS; MALE; MEDICAL RECORD; PHENOTYPE; SKULL BASE;

ACROCEPHALOSYNDACTYLIA; ADOLESCENT; ADULT; CEREBRAL VEINS; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL DYSOSTOSIS; CRANIOSYNOSTOSES; FEMALE; HUMAN; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; MUTATION; PHENOTYPE; RECEPTORS, FIBROBLAST GROWTH FACTOR; SKULL BASE; SUPPORT, NON-U.S. GOV'T; TOMOGRAPHY, X-RAY COMPUTED;

EID: 0033772008     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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