Matches in Nanopublications for { ?s ?p "[Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_assertion description "[Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524860.RA-5J2uHqgFdC1uoxe4Le_mxN_6zIKunV4yWVhlHST2nM130_provenance.