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artigo científico 2011年の論文 2011年学术文章 2011年學術文章 wissenschaftlicher Artikel bài báo khoa học artículu científicu επιστημονικό άρθρο naučni članak tieteellinen artikkeli مقالة علمية نشرت في يوليو 2011 научна статия наукова стаття, опублікована в липні 2011 teaduslik artikkel 2011年學術文章 2011年学术文章 জুলাই ২০১১-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ artikulong pang-agham scientific article published in July 2011 מאמר מדעי articolo scientifico scientific article published in July 2011 vitskapeleg artikkel 2011年學術文章 2011년 논문 article scientifique научни чланак artikel ilmiah tudományos cikk სამეცნიერო სტატია 2011 nî lūn-bûn 2011年學術文章 2011年学术文章 artigo científico 2011年学术文章 article científic мақолаи илмӣ article scientific wetenschappelijk artikel научни чланак artikull shkencor scienca artikolo scientific article published in July 2011 vitenskapelig artikkel 2011年学术文章 videnskabelig artikel vědecký článek научная статья articol științific vetenskaplig artikel artykuł naukowy artigo científico 2011年學術文章 vedecký článok artículo científico publicado en 2011 2011年学术文章 บทความทางวิทยาศาสตร์ bilimsel makale
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Annik Hauri-Hohl Monika Meyer-Böni Eugen J Schoenle Anna Biason-Lauber Mariarosaria Lang-Muritano Mathias Hauri-Hohl
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Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene
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Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene
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Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene
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Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene
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