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мақолаи илмӣ наукова стаття, опублікована в липні 2009 wetenschappelijk artikel (gepubliceerd op 2009-07) scientific article 2009年论文 مقالهٔ علمی artigo científico บทความทางวิทยาศาสตร์ 2009 թվականի հուլիսին հրատարակված գիտական հոդված 2009年論文 научни чланак ২০০৯-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2009年论文 vitskapeleg artikkel bilimsel makale article scientific artykuł naukowy مقالة علمية (نشرت في يوليو 2009) επιστημονικό άρθρο 2009年論文 artículo científico publicado en 2009 vědecký článek publikovaný v roce 2009 سائنسی مضمون tudományos cikk articolo scientifico (pubblicato il 2009-07) 2009年论文 научная статья artikulong pang-agham vitenskapelig artikkel vedecký článok (publikovaný 2009-07) artigo científico (publicado na 2009) научни чланак (објављен 2009-07) articol științific wissenschaftlicher Artikel (veröffentlicht in Juli 2009) videnskabelig artikel (udgivet 2009-07) 2009年論文 מאמר מדעי scienca artikolo 2009년 논문 tieteellinen artikkeli bài báo khoa học artículu científicu espublizáu en 2009 мақолаи илмӣ 2009年论文 teaduslik artikkel 2009年论文 2009年論文 article científic mokslinis straipsnis სამეცნიერო სტატია 2009年の論文 2009年論文 научна статия artikull shkencor artigo científico (publicado na 2009-07) 2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած vetenskaplig artikel 2009年论文 2009 nî lūn-bûn naučni članak article scientifique (publié 2009-07)
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WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
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WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
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WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
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WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes
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