Matches in Nanopublications for { ?s ?p "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695226.RAt9YLIhc4dvswkQtgD529TJE35QzSlhn6wTNqKjKMr1c130_provenance.
- NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278517.RARmH9C9One0ZMGV1I2jA94RRLTU2OL8yeOastigVnXI4130_provenance.
- NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_assertion description "[We report a rare case of double heterozygous type I protein C deficiency and factor V Leiden in a patient with classic myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391723.RAITUUGAOmrWV3UG3P94WMZUnJc3RnqO3j62ZhpQTrW4E130_provenance.