Matches in Nanopublications for { ?s ?p "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409450.RAsNMRcOUopm4NM70ai1H0yAmzaQux0V1-v2HkKt8g68Y130_provenance.
- assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.