Matches in Nanopublications for { ?s ?p "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP670846.RAWlEMETr-CSLanJIN6mWZapbJBp9SP-t9cW9KQ1CRdUk130_assertion description "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670846.RAWlEMETr-CSLanJIN6mWZapbJBp9SP-t9cW9KQ1CRdUk130_provenance.
- NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_assertion description "[High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670847.RAwTGy8brt1mxVb3Na8dKgEwFmALDAt9awVRzWE1wA-pk130_provenance.