Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

Nature Genetics

Volumn 14, Issue 2, 1996, Pages 174-176

  Bellus, G A ^a   Gaudenz, K ^a   Zackai, E H ^a   Clarke, L A ^a   Szabo, J ^a   Francomano, C A ^a   Muenke, M ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 10; CHROMOSOME 8; CRANIOFACIAL SYNOSTOSIS; GENE MUTATION; HUMAN; HUMAN CELL; INFECTIOUS MONONUCLEOSIS; PRIORITY JOURNAL; RECEPTOR GENE;

ACROCEPHALOSYNDACTYLIA; AMINO ACID SEQUENCE; CRANIOFACIAL DYSOSTOSIS; CRANIOSYNOSTOSES; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, DOMINANT; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; POINT MUTATION; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; SYNDROME;

EID: 0029798614     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1096-174     Document Type: Article

References (0)