Matches in Nanopublications for { ?s ?p "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP957739.RAQHN95PxZAOtVJlOt4cK3eaZlQ656ncjY845uxVGqy38130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP957739.RAQHN95PxZAOtVJlOt4cK3eaZlQ656ncjY845uxVGqy38130_provenance.
- assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP924990.RAe_CefCRM4UwOgClskn45vgBwkYL96NlBoYNl-siC07Y130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924990.RAe_CefCRM4UwOgClskn45vgBwkYL96NlBoYNl-siC07Y130_provenance.
- NP924993.RAeubWdBFrgR1B4BUDKdq8I6L8EHWHzsrRdkqyGnsHvQ4130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924993.RAeubWdBFrgR1B4BUDKdq8I6L8EHWHzsrRdkqyGnsHvQ4130_provenance.
- NP924997.RAerZmt5_1hLOSYDFtamXVivfHjj3q3KobUhh8UOYi8K8130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924997.RAerZmt5_1hLOSYDFtamXVivfHjj3q3KobUhh8UOYi8K8130_provenance.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- NP844299.RAsA6XZimt2Ta-Vvq7wqCxuI6tyb8MhUlX6Uximn9ASYw130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844299.RAsA6XZimt2Ta-Vvq7wqCxuI6tyb8MhUlX6Uximn9ASYw130_provenance.
- NP844408.RAmjqk6FM5sQH2_jQTIKjFMjBvnQq_8TEBvdOkJKcL4uE130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844408.RAmjqk6FM5sQH2_jQTIKjFMjBvnQq_8TEBvdOkJKcL4uE130_provenance.
- NP924992.RAtwzCzK46AFAUmWjTKd3ONrE0-R3RMwWpZv5qPx_OZbY130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924992.RAtwzCzK46AFAUmWjTKd3ONrE0-R3RMwWpZv5qPx_OZbY130_provenance.
- NP924991.RAGq42-KXhaHiBGgc8zBPVsv0_miW16q0rvQu4_EHEWy4130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924991.RAGq42-KXhaHiBGgc8zBPVsv0_miW16q0rvQu4_EHEWy4130_provenance.
- NP844387.RA-IOSpE37gb_UhZcAGxm14DYY09QiViGcxh7cZssBBRY130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844387.RA-IOSpE37gb_UhZcAGxm14DYY09QiViGcxh7cZssBBRY130_provenance.