Fronto-Ocular syndrome: Newly recognized trigonocephaly syndrome

American Journal of Medical Genetics

Volumn 93, Issue 2, 2000, Pages 89-93

  Wenstrom, Katharine D ^a   Johanning, Gary L ^a   Owen, John ^a   Johnston, Kelley E ^a   Acton, Shannon ^a   Cliver, Susan ^a   Tamura, Tsunenobu ^a  

^a UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Autosomal dominant inheritance; Craniosynostosis; Fibroblast growth factor receptors; Multiple congenital anomalies; Trigonocephaly

Indexed keywords

FIBROBLAST GROWTH FACTOR 1; FIBROBLAST GROWTH FACTOR 2;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; CRANIOFACIAL SYNOSTOSIS; EPICANTHUS; EXOPHTHALMOS; EYE MALFORMATION; FEMALE; GENE MUTATION; HUMAN; HYPOTELORISM; PALATE MALFORMATION; PRIORITY JOURNAL; PTOSIS;

ADULT; CHILD; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; CRANIOSYNOSTOSES; DEVELOPMENTAL DISABILITIES; FEMALE; FOLLOW-UP STUDIES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; NOSE; PEDIGREE; SYNDROME;

EID: 0034679888     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20000717)93:2<89::aid-ajmg2>3.0.co;2-4     Document Type: Article

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