Matches in Nanopublications for { ?s ?p "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP122104.RAR8ivrimMlvaIWVff4zB_1CGcfXrP_4q4UCu_GDvAV48130_assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122104.RAR8ivrimMlvaIWVff4zB_1CGcfXrP_4q4UCu_GDvAV48130_provenance.
- NP122174.RAULk9pZONghuXptuvTw1EZCjMM-JxO2yKFQlxz3usEsA130_assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122174.RAULk9pZONghuXptuvTw1EZCjMM-JxO2yKFQlxz3usEsA130_provenance.
- NP185292.RAeOdbLTMA14L_3vV2vwNNFwUauXNDrktcLh5DTIumUOQ130_assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185292.RAeOdbLTMA14L_3vV2vwNNFwUauXNDrktcLh5DTIumUOQ130_provenance.
- NP237397.RAWVdU0gsN_81RVl3FeSVye8e81opoIOmmKkIo2qggpQU130_assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237397.RAWVdU0gsN_81RVl3FeSVye8e81opoIOmmKkIo2qggpQU130_provenance.
- assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_assertion description "[we describe a large atypical Holt-Oram syndrome family with mild skeletal deformations and paroxysmal atrial fibrillation, but few have congenital heart disease/of TBX5 revealed a novel mutation, c.373G > A, resulting in p.Gly125Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237396.RAJcEgXgDUFvuCY5yoqum6nZPRvZWdKa60e9Ovz5onOlA130_provenance.