Mutations in fibroblast growth factor receptor 2 gene and craniosynostotic syndromes in Japanese children

Journal of Craniofacial Surgery

Volumn 9, Issue 2, 1998, Pages 162-170

  Nagase, Takashi ^a   Nagase, Miki ^b   Hirose, Shigehisa ^b   Ohmori, Kitaro ^a  

^a TOKYO METROPOLITAN POLICE HOSPITAL   (Japan)

^b TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

Acrocephalosyndactyly; Apert's syndrome; Craniosynostosis; Crouzon's syndrome; Fibroblast growth factor receptor 2; Pfeiffer's syndrome

Indexed keywords

FIBROBLAST GROWTH FACTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR;

ACROCEPHALOSYNDACTYLY; ARTICLE; CHILD; CLINICAL ARTICLE; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; HUMAN; JAPAN; MALE; MORPHOGENESIS; PRIORITY JOURNAL; RECEPTOR GENE;

EID: 0031899314     PISSN: 10492275     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001665-199803000-00015     Document Type: Article

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