A 2.0Mb microdeletion in proximal chromosome 14q12, involving regulatory elements of FOXG1, with the coding region of FOXG1 being unaffected, results in severe developmental delay, microcephaly, and hypoplasia of the corpus callosum

Masaki Takagi, Goro Sasaki, Toshikatsu Mitsui, Misa Honda, Yoko Tanaka, Tomonobu Hasegawa

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