Matches in Nanopublications for { ?s ?p "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP780571.RAq7fQS1Gj3nHZ2nnwAnsWB4A1fiD7RB23WC9uMHZYoOU130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780571.RAq7fQS1Gj3nHZ2nnwAnsWB4A1fiD7RB23WC9uMHZYoOU130_provenance.
- NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428870.RA-gquYc5xpXWgdAtZBc96lUc9mJdzQ7ae43dGJBDeNVk130_provenance.
- NP368058.RAM5gdRNVYCsXugW8tnXDCmVPbXEwOekA72wIX_W7jl4E130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368058.RAM5gdRNVYCsXugW8tnXDCmVPbXEwOekA72wIX_W7jl4E130_provenance.
- NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621019.RALz7cBhwMs-WbKd1QhJxfBTt2iLyfw73YoeGl90sEidY130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP258811.RA9p776ZUdPUP1uBGC60aW7rXvJcGigw9kGDCmDtD_FhQ130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258811.RA9p776ZUdPUP1uBGC60aW7rXvJcGigw9kGDCmDtD_FhQ130_provenance.
- NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258813.RAScp_BZhYq6RL2b7PCTjeCwhJ1YKgzuo_X55NVcbztDQ130_provenance.
- NP408714.RAlgdcGpzhqSEYxhdIqjJrXqMX4hk-2yF3_B_5urtUSpw130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408714.RAlgdcGpzhqSEYxhdIqjJrXqMX4hk-2yF3_B_5urtUSpw130_provenance.