Matches in Nanopublications for { ?s ?p "[Mutations in SMC3 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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- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion description "[Mutations in SMC3 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." NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP153755.RAqrYoTKcdtQwHyiRQ7zmZ2UReU1kjjUwxswblV5UkB-0130_assertion description "[Mutations in SMC3 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." NP153755.RAqrYoTKcdtQwHyiRQ7zmZ2UReU1kjjUwxswblV5UkB-0130_provenance.
- NP222518.RATmuxQx_49psA9SabGeu_F5XAx0Uye45xx0CqAfIR--4130_assertion description "[Mutations in SMC3 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." NP222518.RATmuxQx_49psA9SabGeu_F5XAx0Uye45xx0CqAfIR--4130_provenance.
- NP189979.RAPyJ0c2vv8EmVU-zGcCHpBaPZFVBxhV2kNIFKPl2n75c130_assertion description "[Mutations in SMC3 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." NP189979.RAPyJ0c2vv8EmVU-zGcCHpBaPZFVBxhV2kNIFKPl2n75c130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion description "[Mutations in SMC3 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." NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.