Clinicogenetic study of turkish patients with syndromic craniosynostosis and literature review

Pediatric Neurology

Volumn 50, Issue 5, 2014, Pages 482-490

  Nur, Banu G ^a   Pehlivanoǧlu, Suray ^a   Mihçi, Ercan ^a   Çalişkan, Mualla ^a   Demir, Durkadin ^a   Alper, Özgül M ^a   Kayserili, Hülya ^b   Lüleci, Güven ^a  

^a AKDENIZ UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Apert syndrome; craniosynostosis; Crouzon syndrome; DHPLC; Pfeiffer syndrome

Indexed keywords

FGFR2 PROTEIN, HUMAN; FIBROBLAST GROWTH FACTOR RECEPTOR 2;

ACROCEPHALOSYNDACTYLY; ADOLESCENT; ADULT; CHILD; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; EXON; FEMALE; GENETICS; HUMAN; INFANT; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; YOUNG ADULT;

ACROCEPHALOSYNDACTYLIA; ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL DYSOSTOSIS; CRANIOSYNOSTOSES; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; INFANT; MALE; MUTATION; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; YOUNG ADULT;

EID: 84898792375     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2014.01.023     Document Type: Article

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