Craniosynostosis syndromes in the genomic era

Seminars in Pediatric Neurology

Volumn 11, Issue 4, 2004, Pages 256-261

  Aleck, Kirk ^a  

^a ST JOSEPH'S HOSPITAL AND MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 1; FIBROBLAST GROWTH FACTOR RECEPTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR 3;

ACANTHOSIS NIGRICANS; ACHONDROPLASIA; ACROCEPHALOSYNDACTYLY; BEARE STEVENSON SYNDROME; BRACHYCEPHALY; CRANIAL NEUROPATHY; CRANIAL SUTURE; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; DEVELOPMENTAL DISORDER; DIAGNOSTIC APPROACH ROUTE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; HUMAN; HYDROCEPHALUS; INTRACRANIAL HYPERTENSION; JACKSON WEISS SYNDROME; MENTAL DEFICIENCY; METABOLIC DISORDER; MOLECULAR BIOLOGY; MUENKE SYNDROME; MUTATIONAL ANALYSIS; NEUROPATHOLOGY; PHENOTYPE; PLAGIOCEPHALY; REVIEW; SYMPTOMATOLOGY; SYNDROME;

EID: 15044351458     PISSN: 10719091     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.spen.2004.10.005     Document Type: Review

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