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Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities

M. Seong, S. Park, J. Chae, 2015, Brain and Development.

FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome

J. Chae, Ki Joong Kim, Y. Hwang, 2015, Child neurology open.