Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP700358.RAXhPdJrHtx5GY5WqoymXXa42aWYG9BbSmpt5Wiz-nYyM130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700358.RAXhPdJrHtx5GY5WqoymXXa42aWYG9BbSmpt5Wiz-nYyM130_provenance.
• NP344975.RAiv-ax6SjB7Xj0SjRTrlye9JLpANsYvL3S0BnwgT4AFo130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344975.RAiv-ax6SjB7Xj0SjRTrlye9JLpANsYvL3S0BnwgT4AFo130_provenance.
• NP349866.RAA8LVXWwuyL6QrQix7cEPIGjHM4HgnEuxEl3zu21Qffw130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349866.RAA8LVXWwuyL6QrQix7cEPIGjHM4HgnEuxEl3zu21Qffw130_provenance.
• NP689759.RAt9ycPQgoKCMJGKwrCrkZZdg8Ot4IEmbPFACwj_smUxo130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689759.RAt9ycPQgoKCMJGKwrCrkZZdg8Ot4IEmbPFACwj_smUxo130_provenance.
• NP853003.RAuDVVwWSww0x-5C59zrXq27REl0gV23MzEhEUbDdnhZU130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853003.RAuDVVwWSww0x-5C59zrXq27REl0gV23MzEhEUbDdnhZU130_provenance.
• NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
• NP801304.RASxhZGiMFS-V8QgQ8-iXFgM14YYr5xNmNk6r4zVzzO3k130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801304.RASxhZGiMFS-V8QgQ8-iXFgM14YYr5xNmNk6r4zVzzO3k130_provenance.
• NP800045.RAUYH4G3LmF3ChB6mOYuFuI01QiU1hJJF1TtMJdO90KTQ130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800045.RAUYH4G3LmF3ChB6mOYuFuI01QiU1hJJF1TtMJdO90KTQ130_provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP763067.RAnII1EhAVXCznMqb4O2liMuZnF69y_I0rASE9qZDy3yw130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763067.RAnII1EhAVXCznMqb4O2liMuZnF69y_I0rASE9qZDy3yw130_provenance.
• NP588856.RAdqGalZEuiL5GaiBe__jtbCIXwOHKWkuP_I4-IFK-1JE130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588856.RAdqGalZEuiL5GaiBe__jtbCIXwOHKWkuP_I4-IFK-1JE130_provenance.
• NP588857.RAcxXW8yoCaoGJ97mxpYViyfV3zEQode-7tyWnzJE2F9g130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588857.RAcxXW8yoCaoGJ97mxpYViyfV3zEQode-7tyWnzJE2F9g130_provenance.
• NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588860.RATZQoQ7OAKyTQWnmfgy7Ocs3gEOQbPKpeG2I8NNndZ2s130_provenance.
• NP588861.RAcpR38qWdf2JMe7v84kbsKxKduv3T0vHwGcR1MvGbfFY130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588861.RAcpR38qWdf2JMe7v84kbsKxKduv3T0vHwGcR1MvGbfFY130_provenance.
• NP800071.RAom4OvMl-ouq4IbAVtDOpPWTnguL1FoxSOv3XJLFOyuY130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800071.RAom4OvMl-ouq4IbAVtDOpPWTnguL1FoxSOv3XJLFOyuY130_provenance.
• NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.
• NP588864.RALfy6wyW4NjggdGN1ZxgNgNJdmciLACIQBIE9oxEOiDs130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588864.RALfy6wyW4NjggdGN1ZxgNgNJdmciLACIQBIE9oxEOiDs130_provenance.
• NP763044.RAJRzDYcA7MlKcnTarOqnLYGluGDEH_A2A7ssXmrUhLcQ130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763044.RAJRzDYcA7MlKcnTarOqnLYGluGDEH_A2A7ssXmrUhLcQ130_provenance.
• NP799963.RAMHwjq2QzvIw6g8GgELLBcFEoCNlrduGwZ8zOIkMQVb0130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799963.RAMHwjq2QzvIw6g8GgELLBcFEoCNlrduGwZ8zOIkMQVb0130_provenance.
• NP762942.RA1qDqGC4cSAGCTbf-zulHUijV_bjMLr7-f6ZSwxo7WaY130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762942.RA1qDqGC4cSAGCTbf-zulHUijV_bjMLr7-f6ZSwxo7WaY130_provenance.
• NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.