Matches in Nanopublications for { ?s ?p "[Thus, even important for cardiac development, germline mutations in NKX2.5 are rare in patients with sporadic CHD and genetic and/or pathophysiologic heterogeneity is likely for sporadic forms of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_assertion description "[Thus, even important for cardiac development, germline mutations in NKX2.5 are rare in patients with sporadic CHD and genetic and/or pathophysiologic heterogeneity is likely for sporadic forms of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811125.RAqM2quBszHW5UD_F582WgUPeq5CokU1XabZaXb01EWHA130_provenance.
- NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_assertion description "[Thus, even important for cardiac development, germline mutations in NKX2.5 are rare in patients with sporadic CHD and genetic and/or pathophysiologic heterogeneity is likely for sporadic forms of CHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333982.RAHBi1rR-CT7HvmtuvS7GIcp_nju9vBOSKyQSIad2gMqU130_provenance.