खोज परिणाम - Jong Rak Choi

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    Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy द्वारा Junghan Lee, Sungji Ha, Seung-Tae Lee, Sung-Gyun Park, Saeam Shin, Jong Rak Choi, Keun-Ah Cheon

    प्रकाशित 2020
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    The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report द्वारा Gi-Sung Nam, John Hoon Rim, Jae Young Choi, Heon Yung Gee, Jong Rak Choi, Seung-Tae Lee, Jinsei Jung

    प्रकाशित 2019
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    Clinical Features and Treatment Efficacy in Mutation-Related Epileptic Encephalopathy in the Infant द्वारा Chung Mo Koo, Se Hee Kim, Heung Dong Kim, Joon Soo Lee, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Kang

    प्रकाशित 2019
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    Analysis of trio test in neurodevelopmental disorders द्वारा Se Hee Kim, Soon Sung Kwon, Joon Soo Lee, Heung Dong Kim, Seung-Tae Lee, Jong Rak Choi, Saeam Shin, Hoon-Chul Kang

    प्रकाशित 2022
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