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artigo científico naučni članak teaduslik artikkel 2007年论文 scientific article научная статья наукова стаття, опублікована у квітні 2007 tudományos cikk سائنسی مضمون wetenschappelijk artikel (gepubliceerd in 2007-04) 2007年論文 научни чланак (објављен 2007-04) научни чланак 2007年論文 mokslinis straipsnis vedecký článok (publikovaný 2007-04) artículu científicu espublizáu en 2007 tieteellinen artikkeli мақолаи илмӣ 2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած مقالهٔ علمی artikulong pang-agham artigo científico (publicado na 2007-04) სამეცნიერო სტატია 2007年論文 ২০০৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ wissenschaftlicher Artikel (veröffentlicht in April 2007) videnskabelig artikel (udgivet 2007-04) 2007年论文 vědecký článek publikovaný v roce 2007 article scientific artigo científico (publicado na 2007) 2007 nî lūn-bûn artykuł naukowy vitskapeleg artikkel 2007年论文 2007年论文 2007 թվականի ապրիլին հրատարակված գիտական հոդված article científic vetenskaplig artikel vitenskapelig artikkel 2007年論文 bài báo khoa học мақолаи илмӣ מאמר מדעי научна статия articolo scientifico (pubblicato il 2007-04) 2007年論文 scienca artikolo επιστημονικό άρθρο article scientifique (publié 2007-04) artículo científico publicado en 2007 articol științific مقالة علمية (نشرت في أبريل 2007) bilimsel makale 2007年论文 บทความทางวิทยาศาสตร์ 2007년 논문 artikull shkencor 2007年の論文 2007年论文
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A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
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A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
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A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
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