Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP349469.RATwvJTY338hW_2NM16FX5HOYVNkC2sEWJPny26HJpDjk130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349469.RATwvJTY338hW_2NM16FX5HOYVNkC2sEWJPny26HJpDjk130_provenance.
• NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540702.RA4nOmWmkR9YVPJXGDzmWetiBnhjHEWv-OPI1svgH3xd8130_provenance.
• NP978062.RAflIl4gwr-W3lxsxsiJNLosluKxXvZrSkuCPOFCtV42s130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978062.RAflIl4gwr-W3lxsxsiJNLosluKxXvZrSkuCPOFCtV42s130_provenance.
• assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978035.RAkCesZPE5GTtSUNJY9w3Y9wIhzyPcSn7II2E97BXN2Vw130_provenance.
• NP857499.RAvw1H8nrN-j2Z8Z8WMcMde7ACEwTVxVJv-FUCw1q0et8130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857499.RAvw1H8nrN-j2Z8Z8WMcMde7ACEwTVxVJv-FUCw1q0et8130_provenance.
• NP978058.RAKSeoVZCzncWYKvcM9fWcx4P27soW9tKcYFnGaY4J3LU130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978058.RAKSeoVZCzncWYKvcM9fWcx4P27soW9tKcYFnGaY4J3LU130_provenance.
• NP857497.RAHUZZToL3NZqlqANDpJVwgNvWkaLp0QWzBdXwBfagsu8130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857497.RAHUZZToL3NZqlqANDpJVwgNvWkaLp0QWzBdXwBfagsu8130_provenance.
• NP857498.RAKsL0K4147LdaQsAfTfR7JMy1qp_zw_0-wCcfk-iFiDM130_assertion description "[We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857498.RAKsL0K4147LdaQsAfTfR7JMy1qp_zw_0-wCcfk-iFiDM130_provenance.