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wissenschaftlicher Artikel artikulong pang-agham наукова стаття, опублікована в червні 2017 vědecký článek articolo scientifico 2017 ജൂണ്‍ 30 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം artykuł naukowy scientific article published on 30 June 2017 vitskapeleg artikkel artículo científico publicado en 2017 2017년 논문 2017年学术文章 article scientific 2017年の論文 2017年學術文章 naučni članak tieteellinen artikkeli scienca artikolo vitenskapelig artikkel научна статия 2017年学术文章 2017年学术文章 vetenskaplig artikel научни чланак מאמר מדעי article scientifique artikull shkencor 2017年學術文章 article científic مقالة علمية نشرت في 30 يونيو 2017 научни чланак επιστημονικό άρθρο 2017年学术文章 artigo científico teaduslik artikkel scientific article published on 30 June 2017 tudományos cikk 2017年学术文章 ৩০ জুন ২০১৭-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2017 nî lūn-bûn videnskabelig artikel wetenschappelijk artikel scientific article published on 30 June 2017 bài báo khoa học мақолаи илмӣ artigo científico articol științific 2017年学术文章 სამეცნიერო სტატია 2017年學術文章 artikel ilmiah artículu científicu bilimsel makale научная статья บทความทางวิทยาศาสตร์ 2017年學術文章 artigo científico vedecký článok 2017年學術文章
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Hannah Tamary Sharon Noy-Lotan Tanya Krasnov Vijay G Sankaran Orly Dgany Dina Attias Orna Steinberg-Shemer Ruth Laor
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Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.
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Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.
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Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia. Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.
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Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia.
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