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2012年论文 vedecký článok vitskapeleg artikkel tieteellinen artikkeli wissenschaftlicher Artikel 2012年论文 artigo científico naučni članak مقالة علمية نشرت في 12 سبتمبر 2012 2012년 논문 2012年の論文 vědecký článek vetenskaplig artikel מאמר מדעי artikull shkencor artigo científico articol științific 2012年論文 บทความทางวิทยาศาสตร์ ১২ সেপ্টেম্বর ২০১২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ научна статия 2012年论文 научни чланак 2012年論文 2012 թվականի սեպտեմբերի 12-ին հրատարակված գիտական հոդված wetenschappelijk artikel 2012年论文 наукова стаття, опублікована у вересні 2012 article científic научни чланак scientific article published on 12 September 2012 2012年论文 2012 nî lūn-bûn artikel ilmiah artículu científicu espublizáu en 2012 article scientific artykuł naukowy artigo científico scienca artikolo 2012年論文 2012年論文 artikulong pang-agham videnskabelig artikel სამეცნიერო სტატია επιστημονικό άρθρο artículo científico publicado en 2012 2012年論文 tudományos cikk article scientifique 2012年论文 vitenskapelig artikkel scientific article published on 12 September 2012 articolo scientifico bilimsel makale teaduslik artikkel scientific article published on 12 September 2012 мақолаи илмӣ научная статья bài báo khoa học
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Felicity Collins Kerry Fagan Gladys Ho Elisa Bettella Alisa Knapman Gregory B Peters Artur Darmanian Fiona McKenzie Carolyn J Ellaway Anna Hackett
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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
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