Matches in Nanopublications for { ?s ?p "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP465610.RAfhbrbmYwgO0CYiNfB2BKvxuhiaAMnNFKGAxK0m4ghE8130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465610.RAfhbrbmYwgO0CYiNfB2BKvxuhiaAMnNFKGAxK0m4ghE8130_provenance.
- assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674781.RAaL8MSNbH5XaeH-B246mh7Yry41alTRTHYXxgW6GNUSc130_provenance.
- NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612512.RAPspVmyGRLJVxEG3MahetSCPZjrtp5IyJppltvNAKDQY130_provenance.
- NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674783.RAIVEjVzCmgx4kWQRZXb0j3PIEyPImUmEK1VMZjbjVgCM130_provenance.
- NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP679962.RAxxRE8fFz1yOXwQVVzpTxxdI00E_mrTmBgnRSHw5Ogaw130_provenance.
- NP674780.RA32JjDdNV6Y2qgHLwxJp18qT5uE7h3VBkqK2Nzq7vhpo130_assertion description "[In this article, we report the identification of four new dyslexia candidate genes (PCNT, DIP2A, S100B, and PRMT2) on chromosome region 21q22.3 by FISH and SNP microarray analyses of a very small deletion in this region, which cosegregates with dyslexia in a father and his three sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674780.RA32JjDdNV6Y2qgHLwxJp18qT5uE7h3VBkqK2Nzq7vhpo130_provenance.