Matches in Wikidata for { <http://www.wikidata.org/entity/Q46668071> ?p ?o ?g. }
- Q46668071 description "2015 nî lūn-bûn" @default.
- Q46668071 description "2015年の論文" @default.
- Q46668071 description "2015年学术文章" @default.
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- Q46668071 description "2015年学术文章" @default.
- Q46668071 description "2015年学术文章" @default.
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- Q46668071 description "2015年學術文章" @default.
- Q46668071 description "2015年學術文章" @default.
- Q46668071 description "2015年學術文章" @default.
- Q46668071 description "2015年學術文章" @default.
- Q46668071 description "2015년 논문" @default.
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- Q46668071 description "artículo científico publicado en 2015" @default.
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- Q46668071 description "bilimsel makale" @default.
- Q46668071 description "bài báo khoa học" @default.
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- Q46668071 description "scientific article published on 28 April 2015" @default.
- Q46668071 description "scientific article published on 28 April 2015" @default.
- Q46668071 description "scientific article published on 28 April 2015" @default.
- Q46668071 description "teaduslik artikkel" @default.
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- Q46668071 description "επιστημονικό άρθρο" @default.
- Q46668071 description "мақолаи илмӣ" @default.
- Q46668071 description "наукова стаття, опублікована у квітні 2015" @default.
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- Q46668071 description "מאמר מדעי" @default.
- Q46668071 description "مقالة علمية نشرت في 28 أبريل 2015" @default.
- Q46668071 description "২৮ এপ্রিল ২০১৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q46668071 description "บทความทางวิทยาศาสตร์" @default.
- Q46668071 description "სამეცნიერო სტატია" @default.
- Q46668071 name "Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation" @default.
- Q46668071 name "Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation" @default.
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- Q46668071 label "Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation" @default.
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- Q46668071 prefLabel "Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation" @default.
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- Q46668071 P1476 "Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation" @default.
- Q46668071 P2093 "Catherine Cole" @default.
- Q46668071 P2093 "Elizabeth Davis" @default.
- Q46668071 P2093 "Jayne Houghton" @default.
- Q46668071 P2093 "Mary Abraham" @default.
- Q46668071 P2093 "Richard Loh" @default.
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