Matches in Nanopublications for { ?s ?p "[The involvement of congenital anomalies in all 16 clinically described patients with EP300 mutations (25% of which have been identified by hypothesis free methods, including microarray, exome, and whole-genome sequencing) is reviewed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_assertion description "[The involvement of congenital anomalies in all 16 clinically described patients with EP300 mutations (25% of which have been identified by hypothesis free methods, including microarray, exome, and whole-genome sequencing) is reviewed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266123.RAuDXBjhWLTCvY-sqkUkTDjDHTDZyS4jK0Rvqd9LVuYFM130_provenance.