Sökresultat - Dae-Hyun Jang

NDUFAF6-Related Leigh Syndrome Caused by Rare Pathogenic Variants: A Case Report and the Focused Review of Literature av Jaewon Kim, Jaewoong Lee, Dae-Hyun Jang

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Case Report: Pansynostosis, Chiari I Malformation and Syringomyelia in a Child With Frontometaphyseal Dysplasia 1 av Jaewon Kim, Dong-Woo Lee, Dae-Hyun Jang

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A 3-month-old Infant with Mottled Hypo- and Hyper-pigmented Patches on the Extremities: A Quiz av Suyeon Kim, Dae-Hyun Jang, Hei Sung Kim

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CTNNB1-related neurodevelopmental disorder mimics cerebral palsy: case report av Jaewoong Lee, Jaeeun Yoo, Seungok Lee, Dae-Hyun Jang

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A novel pathogenic variant of DNMT3A associated with craniosynostosis: a case report of Heyn-Sproul-Jackson syndrome av Ga Hye Kim, Jaewon Kim, Jaewoong Lee, Dae-Hyun Jang

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Case Report: Co-occurrence of Duchenne Muscular Dystrophy and Frontometaphyseal Dysplasia 1 av Jaewon Kim, Dong-Woo Lee, Ja-Hyun Jang, Myungshin Kim, Jisook Yim, Dae-Hyun Jang

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The Effect of the 'Touch Screen-Based Cognitive Training' for Children with Severe Cognitive Impairment in Special Education av In Young Sung, Jin Sook Yuk, Dae-Hyun Jang, Gijeong Yun, Chunye Kim, Eun Jae Ko

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Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report av Shin-Hee Kim, Minsung Kim, Jisook Yim, Jisook Yim, Myungshin Kim, Myungshin Kim, Dae-Hyun Jang

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Concurrence of Congenital Muscular Torticollis and Congenital Torticollis Due to Other Anomalies: Two Case Reports av Min-Wook Kim, Da-Ye Kim, Dong-Woo Lee, Da-Hye Ryoo, Jaewon Kim, Dae-Hyun Jang

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Correction to: Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report av Hoo Young Lee, Dae-Hyun Jang, Jae-Won Kim, Dong-Woo Lee, Ja-Hyun Jang, Joungsu Joo

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Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report av Hoo Young Lee, Dae-Hyun Jang, Jae-Won Kim, Dong-Woo Lee, Ja-Hyun Jang, Joungsu Joo

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Two Novel Mutations (c.883-4_890del and c.1684C>G) of WDR62 Gene Associated With Autosomal Recessive Primary Microcephaly: A Case Report av You Gyoung Yi, You Gyoung Yi, Dong-Woo Lee, Jaewon Kim, Ja-Hyun Jang, Ja-Hyun Jang, Sae-Mi Lee, Sae-Mi Lee, Dae-Hyun Jang

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