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http://purl.uniprot.org/citations/15770128http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15770128http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15770128http://www.w3.org/2000/01/rdf-schema#comment"We report a four generation family with features of the facio-audio-symphalangism syndrome. This condition is characterized by proximal symphalangism, conductive hearing loss due to stapes fixation and a distinctive facies. A novel nonsense mutation in the NOG gene on chromosome 17q22 was identified in the patients. The variable expression and progressive nature of the syndrome is well illustrated by this family. The role of Noggin as the causative factor of symphalangism is discussed."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.org/dc/terms/identifier"doi:10.1097/00019605-200504000-00004"xsd:string
http://purl.uniprot.org/citations/15770128http://purl.org/dc/terms/identifier"doi:10.1097/00019605-200504000-00004"xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Vanhoenacker F."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Vanhoenacker F."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Van Hul E."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Van Hul E."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Declau F."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Declau F."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Baten E."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Baten E."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Claes J."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Claes J."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Mattelaer P."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"Mattelaer P."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"van den Ende J.J."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/author"van den Ende J.J."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/name"Clin. Dysmorphol."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/name"Clin. Dysmorphol."xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/pages"73-80"xsd:string
http://purl.uniprot.org/citations/15770128http://purl.uniprot.org/core/pages"73-80"xsd:string