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http://purl.uniprot.org/citations/28884947http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28884947http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28884947http://www.w3.org/2000/01/rdf-schema#comment"We present a 4-year-old girl with delayed neuromotor development, short stature of prenatal onset, and specific behavioral and craniofacial features harboring an intragenic deletion in the ARID2 gene. The phenotype confirmed the major features of the recently described ARID2-related intellectual disability syndrome. However, our patient showed overlapping features with Nicolaides-Baraitser syndrome and Coffin-Siris syndrome, providing further arguments to reclassify these disorders as "SWI/SNF-related intellectual disability syndromes.""xsd:string
http://purl.uniprot.org/citations/28884947http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.38407"xsd:string
http://purl.uniprot.org/citations/28884947http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.38407"xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Callewaert B."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Callewaert B."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"D'hondt M."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"D'hondt M."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"De Bruyne P."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"De Bruyne P."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Dheedene A."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Dheedene A."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Fraenkel U."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Fraenkel U."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Menten B."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Menten B."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Van Paemel R."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"Van Paemel R."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"van der Straaten S."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/author"van der Straaten S."xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/28884947http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string