Matches in Nanopublications for { ?s ?p "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP649680.RAM1z3yeNpty3R4qOuAi6yM7gOfoBvif9d8YwTi2JbX6s130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649680.RAM1z3yeNpty3R4qOuAi6yM7gOfoBvif9d8YwTi2JbX6s130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.