Matches in Nanopublications for { ?s ?p "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126817.RAZWxcrg4L6p-G2b5_mHP3Kqe8_VsfS22S3c8XaSOCgK0130_provenance.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.
- NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189998.RAc8nnTU7VxhnKGdYWtKG8eSLA45AQTCotHu-G-2POZ8E130_provenance.
- NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222517.RA3nqwSTZm48rcVX_GGCgpSnvJICIaC3sEamVgo2_iMWw130_provenance.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.