Annals of Child Neurology

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; DOI: https://doi.org/10.26815/acn.2024.00717; Full text PubReader ePub PDF

Deep Phenotyping in 1p36 Deletion Syndrome: Youngkyu Shim, Young Jun Go, Soo Yeon Kim, Hunmin Kim, Hee Hwang, Jieun Choi, Byung Chan Lim, Ki Joong Kim, Jong-Hee Chae; Ann Child Neurol. 2020;28(4):131-137. Published online August 13, 2020; DOI: https://doi.org/10.26815/acn.2020.00108
Cited By 5; Full text PubReader ePub PDF

다양한 유형의 발작을 보인 1p36 결실증후군 1례: J Korean Child Neurol Soc. 2015;23(4):165-169. Published online December 30, 2015; DOI: https://doi.org/10.26815/jkcns.2015.23.4.165; PDF

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