Mutation detection in FGFR2 craniosynostosis syndromes

Human Genetics

Volumn 99, Issue 2, 1997, Pages 251-255

  Hollway, Georgina E ^a,b   Suthers, Graeme K ^a   Haan, Eric A ^a   Thompson, Elizabeth ^a   David, David J ^a   Gecz, Jozef ^a,d   Mulley, John C ^a,c  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^b UNIVERSITY OF ADELAIDE   (Australia)

^c UNIVERSITY OF ADELAIDE   (Australia)

^d INSTITUTE OF MOLECULAR PHYSIOLOGY AND GENETICS   (Slovakia)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ACANTHOSIS NIGRICANS; ACROCEPHALOSYNDACTYLY; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; EXON; GENE MUTATION; HUMAN; PHENOTYPE; PRIORITY JOURNAL; RNA SPLICING;

ADULT; CRANIOSYNOSTOSES; FEMALE; HUMANS; MUTATION; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; SYNDROME;

EID: 0031024743     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050348     Document Type: Article

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