Matches in Nanopublications for { ?s ?p "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756729.RASFaYdN5e9p86P8bzhlXDiG6oeK4pn2MS-7yxOUqM4DA130_provenance.
- assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.