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14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

✍ Scribed by Ellaway, Carolyn J; Ho, Gladys; Bettella, Elisa; Knapman, Alisa; Collins, Felicity; Hackett, Anna; McKenzie, Fiona; Darmanian, Artur; Peters, Gregory B; Fagan, Kerry; Christodoulou, John

Book ID: 118023005
Publisher: Nature Publishing Group
Year: 2012
Tongue: English
Weight: 322 KB
Volume: 21
Category: Article
ISSN: 1018-4813
DOI: 10.1038/ejhg.2012.208

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