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scientific article published on 19 April 2016 vedecký článok 2016年學術文章 tieteellinen artikkeli article scientific tudományos cikk ১৯ এপ্রিল ২০১৬-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ מאמר מדעי articolo scientifico 2016年学术文章 videnskabelig artikel bài báo khoa học სამეცნიერო სტატია articol științific artykuł naukowy artikulong pang-agham scienca artikolo 2016年学术文章 научни чланак 2016年学术文章 bilimsel makale artigo científico artículu científicu scientific article published on 19 April 2016 2016年學術文章 2016年学术文章 vetenskaplig artikel научная статья научни чланак vitskapeleg artikkel 2016年の論文 2016년 논문 scientific article published on 19 April 2016 บทความทางวิทยาศาสตร์ مقالة علمية نشرت في 19 أبريل 2016 vědecký článek artigo científico artikel ilmiah 2016年学术文章 2016年學術文章 мақолаи илмӣ wissenschaftlicher Artikel artikull shkencor vitenskapelig artikkel article científic 2016年學術文章 wetenschappelijk artikel επιστημονικό άρθρο artigo científico 2016年學術文章 teaduslik artikkel научна статия наукова стаття, опублікована у квітні 2016 2016 nî lūn-bûn 2016年学术文章 artículo científico publicado en 2016 article scientifique naučni članak
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Amber Begtrup Wendy K Chung Sara Halbach David B Beck Carin Yates Victoria Sanders Megan T Cho Renkui Bai Francisca Millan Brad Angle Yufeng Shen Bridget O'Connor Anne M Connolly Darrel Waggoner Kyle Retterer Mark Hannibal
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.
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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
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