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Identification of De Novo Radio-Tartaglia Syndrome and Comparison of Clinical and Molecular Characteristics with Those of 1p36 Deletion Syndrome
Hyun-Young Kim, Jeehun Lee, Ja-Hyun Jang, Jong-Won Kim, Jiwon Lee, Mi-Ae Jang
Ann Child Neurol. 2025;33(1):8-15.   Published online December 24, 2024
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Distinctive Severe Ocular Abnormalities and Epilepsy Accompanied by a Novel ZEB2 Mutation in a Child with Mowat-Wilson Syndrome
Soyoung Park, Yun Jung Hur, Jin Sook Yoon, Mi-Ae Jang
Ann Child Neurol. 2022;30(1):31-34.   Published online August 27, 2021
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A Novel Pathogenic Variant (c.592_599del) in PCDH19 in a Korean Family with Epilepsy
You Na Park, Mi-Ae Jang, Soyoung Park
Ann Child Neurol. 2019;27(4):152-154.   Published online December 3, 2019
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