Matches in Nanopublications for { ?s ?p "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545376.RAupywKmsVyoNx9ePzk8MJjTgD5jE7j7Voe3svAZooENI130_provenance.
- NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383035.RAYVlaF6todlMxRAk3C_bHqkd7GOL-iJwbZ59ceOM3Gy4130_provenance.
- NP748253.RAn5zJXIHQnz1gj4uj3JtdEN2-wMNOkoN4eAszhAoF9YE130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748253.RAn5zJXIHQnz1gj4uj3JtdEN2-wMNOkoN4eAszhAoF9YE130_provenance.
- NP253339.RALonHe6PEG7RmHHL6LIpw3emzDWa0xd27zBivq1iyZPk130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253339.RALonHe6PEG7RmHHL6LIpw3emzDWa0xd27zBivq1iyZPk130_provenance.
- NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253393.RAN-IUDBk4mrBLhflIK7YMO5TYegK1tnekHFRYSuE1a-A130_provenance.
- NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion description "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance.