Matches in Nanopublications for { ?s ?p "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP403402.RA20xveDWFYz0D9HnAcj1FAw1032foo_Iln51-CXdL4bY130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403402.RA20xveDWFYz0D9HnAcj1FAw1032foo_Iln51-CXdL4bY130_provenance.
- NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724077.RASDapbIGyQIPAe_eeiTzMbZ9HMFz2_Y40x9985wtlcyE130_provenance.
- NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724144.RAXMD8dLelhDtVXUU_uh9ei0EEF3eLtMlYBXIFDH6dIW8130_provenance.
- NP525840.RAwEgipYDR64NNWZLf12E5s9HLoVGi0Y0LzXBlgXflDRA130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525840.RAwEgipYDR64NNWZLf12E5s9HLoVGi0Y0LzXBlgXflDRA130_provenance.
- assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_assertion description "[Various mutations in the TBX5 gene have been identified in patients with Holt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525837.RAv2Yy4i75AGVUWk7ZD9WyVDXWdmp6BGCagybZSTkZqqs130_provenance.