Matches in Nanopublications for { ?s ?p "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1701.RAFfCjMEfcaosuhesQ9qAyFOXNCBEOyKcaD2A7IP0NPnU130_provenance.
- assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296091.RAMT6ShJT-qXbU_bZkhwuUmAc2dTdPYN18PTwvVtYXoZg130_provenance.
- NP1354.RAGSugf3xeiOHXW3G04vETLNBY4zIPWbJv7VCCMgzpgF8130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354.RAGSugf3xeiOHXW3G04vETLNBY4zIPWbJv7VCCMgzpgF8130_provenance.
- NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6066.RAIczhkx4R_DlqMWq-uDSglbfBzeyncFoEky03P1U95qA130_provenance.
- NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787616.RALj4RFE8r9kYJdLlPvlqOGnpsQRUMhTDVC88tr7mDEuA130_provenance.
- NP787617.RA-U1cqcl1ZxU-fAjgqg22OgqGZqutQmZHBfWM_9DpJx0130_assertion description "[Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787617.RA-U1cqcl1ZxU-fAjgqg22OgqGZqutQmZHBfWM_9DpJx0130_provenance.