Agenesis of the corpus callosum, developmental delay, autism spectrum disorder, facial dysmorphism, and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion
Ayeshah Chaudhry; Brian H. Chung; Dimitri J. Stavropoulos; Marcela P. Araya; Asim Ali; Elise Heon; David Chitayat
Author Information: Department of Laboratory Medicine and Genetics
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