Matches in Nanopublications for { ?s ?p "[Point mutations in TBX1 can recapitulate many of the structural defects of 22q11 deletion syndromes (22q11DS), usually associated with a chromosomal deletion at 22q1.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion description "[Point mutations in TBX1 can recapitulate many of the structural defects of 22q11 deletion syndromes (22q11DS), usually associated with a chromosomal deletion at 22q1.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.