Matches in Nanopublications for { ?s ?p "[Mutations in cohesin complex members SMC3 and 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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- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- assertion description "[Mutations in cohesin complex members SMC3 and 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." provenance.
- assertion description "[Mutations in cohesin complex members SMC3 and 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." provenance.
- assertion description "[Mutations in cohesin complex members SMC3 and 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." provenance.
- NP592061.RADfGbpx46_-6DPQvXP6uzoktfFUJkdiWO_RoVwnT91Ww130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP592061.RADfGbpx46_-6DPQvXP6uzoktfFUJkdiWO_RoVwnT91Ww130_provenance.
- NP815581.RAoOd1weOAv4QE5UPX4J-zGSJw3YqN7KJglASELVOkXIs130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP815581.RAoOd1weOAv4QE5UPX4J-zGSJw3YqN7KJglASELVOkXIs130_provenance.
- NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP592059.RAp2TNURAl0yY4CNbhG4M5xFwHYaXhsjk6vv4A7QO5llg130_provenance.
- NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP592063.RANAifKVJhtkLs7hVh4vVXxQQjSyCpf6qM07ei_wHio3c130_provenance.
- NP592058.RA46RS_AROL7hTT16iQaYG2uuUSM6fhqcdIL_-jRpwtYo130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP592058.RA46RS_AROL7hTT16iQaYG2uuUSM6fhqcdIL_-jRpwtYo130_provenance.