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scientific article published in April 1993 artículo científico publicado en 1993 научна статия artikull shkencor vitenskapelig artikkel vedecký článok 1993年學術文章 1993年学术文章 1993 nî lūn-bûn articol științific научни чланак article scientifique videnskabelig artikel artículu científicu artykuł naukowy мақолаи илмӣ บทความทางวิทยาศาสตร์ article científic artikel ilmiah bài báo khoa học artigo científico 1993年學術文章 مقالة علمية نشرت في أبريل 1993 1993年学术文章 научная статья wetenschappelijk artikel artikulong pang-agham scientific article published in April 1993 1993年學術文章 teaduslik artikkel 1993年学术文章 article scientific bilimsel makale tudományos cikk scienca artikolo wissenschaftlicher Artikel vetenskaplig artikel 1993年学术文章 scientific article published in April 1993 1993년 논문 სამეცნიერო სტატია artigo científico 1993年學術文章 1993年学术文章 naučni članak articolo scientifico এপ্রিল ১৯৯৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ vitskapeleg artikkel vědecký článek 1993年學術文章 tieteellinen artikkeli наукова стаття, опублікована у квітні 1993 1993年の論文 מאמר מדעי artigo científico 1993年学术文章 научни чланак επιστημονικό άρθρο
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D J Prockop J Zhuang K Nakayasu
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Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta. Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2
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Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2 Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta.
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Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta. Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2
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Deletion of 19 base pairs in intron 13 of the gene for the pro alpha 2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta.
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10.1007/BF00218258