Matches in Nanopublications for { ?s ?p "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP317585.RA2hG39GoJPI8QKUpYt1zVNwsVaDMkxQIdGAq9ZFtUA3I130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317585.RA2hG39GoJPI8QKUpYt1zVNwsVaDMkxQIdGAq9ZFtUA3I130_provenance.
- NP615054.RA4_wEqdUN9Y5a3yhQa8dzcBIre-b9hnlrJ9-cRb0yGIE130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615054.RA4_wEqdUN9Y5a3yhQa8dzcBIre-b9hnlrJ9-cRb0yGIE130_provenance.
- assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP404504.RAVW2Z_EiziiSgucS9m5ZHRqsyvGS5lngwOjaHb10-BSk130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404504.RAVW2Z_EiziiSgucS9m5ZHRqsyvGS5lngwOjaHb10-BSk130_provenance.
- NP913418.RA3TzLSd7oBnw_oBxUBmNLihIU258NHfcTxqckvYDGDnw130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913418.RA3TzLSd7oBnw_oBxUBmNLihIU258NHfcTxqckvYDGDnw130_provenance.
- NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725471.RArFWQM8TdOVRfiNV8N0JfhgriiXKXMEX6wILTPWJzia0130_provenance.
- NP725470.RA1LAu81Bfatoi4dBAUJfGmFmyiolBb3xt2eV2daK9Z7M130_assertion description "[After screening for mutations in PAX6, CYP1B1, and FOXC1, a novel FOXC1 W152G mutation was identified in a newborn boy with aniridia and congenital glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725470.RA1LAu81Bfatoi4dBAUJfGmFmyiolBb3xt2eV2daK9Z7M130_provenance.