RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/8676562http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8676562http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8676562http://www.w3.org/2000/01/rdf-schema#comment"Apert syndrome, acrocephalosyndactyly Type I, is an autosomal dominant craniosynostosis comprising acrocephaly, facial dysmorphism and severe syndactyly of the hands and feet. Missense mutations at codons 252 and 253 at 5'-end on exon 7 of fibroblast growth factor receptor (FGFR) 2 have been identified in a large number of patients with Apert syndrome. In this study, nucleotide sequences on the intron 6 were determined by vector ligation-PCR and direct sequencing. Five DNA samples from sporadic Apert syndrome were examined by non-RI SSCP and direct sequencing using a primer pair of intron 6 and exon 7. All cases of the syndrome showed abnormal banding pattern in the SSCP and missense mutations from Ser to Trp at codon 252 of the FGFR2 gene. The non-RI SSCP and direct sequencing of the FGFR2 exon 7 from genomic DNAs may be a useful and rapid molecular means for clinical diagnosis of Apert syndrome."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Yamazaki Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Yamazaki Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Wada C."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Wada C."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Takada F."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Takada F."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ohtani H."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ohtani H."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ohnuki Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ohnuki Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ishigaki M."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Ishigaki M."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Toyo-oka Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Toyo-oka Y."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Yamabe H."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/author"Yamabe H."xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/date"1996"xsd:gYear
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/date"1996"xsd:gYear
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/name"Rinsho Byori"xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/name"Rinsho Byori"xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/pages"435-438"xsd:string
http://purl.uniprot.org/citations/8676562http://purl.uniprot.org/core/pages"435-438"xsd:string