Expression analysis of an FGFR2 IIIc 5' splice site mutation (1084+3A->G).

Journal of medical genetics

Volumn 41, Issue 8, 2004, Pages

  Kan, R ^a   Twigg, S R ^a   Berg, J ^a   Wang, L ^a   Jin, F ^a   Wilkie, A O ^a  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FGFR2 PROTEIN, HUMAN; FIBROBLAST GROWTH FACTOR RECEPTOR; FIBROBLAST GROWTH FACTOR RECEPTOR 2; PROTEIN TYROSINE KINASE;

ALTERNATIVE RNA SPLICING; ARTICLE; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; EXON; FEMALE; GENE EXPRESSION REGULATION; GENETIC SCREENING; GENETICS; HUMAN; MALE; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RNA SPLICING; SYNDROME;

ABNORMALITIES, MULTIPLE; ALTERNATIVE SPLICING; CRANIOFACIAL DYSOSTOSIS; CRANIOSYNOSTOSES; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENE EXPRESSION REGULATION; GENETIC SCREENING; HUMANS; MALE; MUTATION; PEDIGREE; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 2; RECEPTORS, FIBROBLAST GROWTH FACTOR; RNA SPLICE SITES; SYNDROME;

EID: 16544388265     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2004.018507     Document Type: Article

References (0)