Matches in Nanopublications for { ?s ?p "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP901347.RAAKRzwNQQsoYbwE0HC5jY4qD5mZaZQpr77mZJaq1tmw0130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901347.RAAKRzwNQQsoYbwE0HC5jY4qD5mZaZQpr77mZJaq1tmw0130_provenance.
- NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870057.RAvOSBVYQvF_fQstQO_K6iyLnPeK1KdUgHt2Rr-LkO6G0130_provenance.
- NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512334.RA773KN6ZUJF8Tm17oWP_kmokWdh9Cyw2Ic5o87R3IDdU130_provenance.
- NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_assertion description "[To test further for mutant DNAH11 as a cause of PCD, DNAH11 was sequenced in patients with a PCD clinical phenotype, but no known genetic aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675097.RAKQ3YRaXAlzOA529guJgMBLuzV6dbpIn7-R_r-e3zwdA130_provenance.