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บทความทางวิทยาศาสตร์ 2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած vitenskapelig artikkel научна статия מאמר אקדמי vědecký článek publikovaný v roce 2001 artigo científico artículu científicu espublizáu en 2001 bilimsel makale tieteellinen artikkeli 2001年学术文章 vitskapeleg artikkel 2001年学术文章 artikull shkencor 2001年學術文章 article científic scienca artikolo 2001년 논문 2001年学术文章 naučni članak наукова стаття, опублікована у квітні 2001 2001年學術文章 wetenschappelijk artikel (gepubliceerd op 2001/04/20) научни чланак vetenskaplig artikel (publicerad på 2001/04/20) teaduslik artikkel مقالة علمية (نشرت في 20-4-2001) 2001年學術文章 mokslinis straipsnis სამეცნიერო სტატია научни чланак (објављен 2001/04/20) artigo científico (publicado na 2001/04/20) ശാസ്ത്ര പ്രബന്ധം article scientific научная статья tudományos cikk articolo scientifico (pubblicato il 2001/04/20) 2001 թվականի ապրիլին հրատարակված գիտական հոդված articol științific scientific article artigo científico (publicado na 2001) мақолаи илмӣ 2001 nî lūn-bûn 2001年学术文章 мақолаи илмӣ artikulong pang-agham artículo científico publicado en 2001 مقالهٔ علمی 2001年學術文章 artykuł naukowy wissenschaftlicher Artikel (veröffentlicht am 20 April 2001) 2001年の論文 vedecký článok (publikovaný 2001/04/20) επιστημονικό άρθρο article scientifique (publié 2001/04/20) ২০০১-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2001年学术文章 2001年學術文章 videnskabelig artikel (udgivet 2001/04/20) 2001年學術文章 bài báo khoa học سائنسی مضمون
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COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II
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COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II
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COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II
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