Matches in Nanopublications for { ?s ?p "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660161.RASSJlNraFwP8fp-cLxPLirL5WFotnBW4s6Y9Ory6Q4bU130_provenance.
- NP647832.RAvEkbPEmljgIT1BwCFceTX3QhnvGbcpeW7M6ziNX4L6U130_assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647832.RAvEkbPEmljgIT1BwCFceTX3QhnvGbcpeW7M6ziNX4L6U130_provenance.
- NP444463.RAwsZ0J-5L1IlDPtYIXRwQNnRMf9x_dp_TAAylJZTeZlk130_assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444463.RAwsZ0J-5L1IlDPtYIXRwQNnRMf9x_dp_TAAylJZTeZlk130_provenance.
- NP650540.RAOe1DHo2GGIdv1gKZJdgizQNuSdyB0OlU6ZjYk0D1CFA130_assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650540.RAOe1DHo2GGIdv1gKZJdgizQNuSdyB0OlU6ZjYk0D1CFA130_provenance.
- assertion description "[PCH is most often autosomal recessive though de novo anomalies in the X-linked gene CASK have recently been identified in patients, mostly females, presenting with intellectual disability, microcephaly and PCH (MICPCH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.