Matches in Nanopublications for { ?s ?p "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP426231.RAn2bEQ6QT2pbNhBfSdaK0aR9cJqpNbUrZ71f65WD_GQQ130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426231.RAn2bEQ6QT2pbNhBfSdaK0aR9cJqpNbUrZ71f65WD_GQQ130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP607268.RAUZqEcw8tzV1e45j1sDRELMXxe-VT88ELIiXie5MyQJE130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607268.RAUZqEcw8tzV1e45j1sDRELMXxe-VT88ELIiXie5MyQJE130_provenance.
- NP607271.RAVotBcTHuroYQLqFBo-AkSFBJTO15lVASAzbHM8VcYpM130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607271.RAVotBcTHuroYQLqFBo-AkSFBJTO15lVASAzbHM8VcYpM130_provenance.
- NP784219.RAn4dbbnd_rSqawa86dmCW9Zmm4JMr4lGMjVpZ-TuhXsk130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784219.RAn4dbbnd_rSqawa86dmCW9Zmm4JMr4lGMjVpZ-TuhXsk130_provenance.