Matches in Nanopublications for { ?s ?p "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP334026.RAXDJXD_S06iiCs7zlJYpjZg_z2ELteNQ3t6ev0VtQdXA130_assertion description "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334026.RAXDJXD_S06iiCs7zlJYpjZg_z2ELteNQ3t6ev0VtQdXA130_provenance.
- NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_assertion description "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496225.RAM3xFq2sm0GKET-bSG-yFHQdw0qNHHAiuiu7a55Q0Cts130_provenance.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion description "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.