Genetic syndromes associated with overgrowth in childhood by Jung Min Ko

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Kabuki syndrome: clinical and molecular characteristics by Chong-Kun Cheon, Jung Min Ko

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Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhood by Hwa Young Kim, Jung Min Ko

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A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up by Jaehui Ryu, Jung Min Ko, Choong-Ho Shin

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Case report: Focal segmental glomerulosclerosis in a pediatric atypical progeroid syndrome by Seoyun Jang, Yo Han Ahn, Yo Han Ahn, Yo Han Ahn, Jung Min Ko, Jung Min Ko, Jung Min Ko, Jae Sung Ko, Sojung Lim, Hee Gyung Kang, Hee Gyung Kang, Hee Gyung Kang

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P357: Clinical and genetic profiling of cleidocranial dysplasia: A comprehensive study of 28 Korean patients by Jung Min Ko, Hyebin Yoo, Naye Choi, Ayoung Park

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P358: Uncovering the clinical spectrum of citrin deficiency in Korea: Insights from a study of 30 patients by Jung Min Ko, Ayoung Park, Naye Choi, Hwa Young Kim

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Flap Extension Technique Using Intrasocket Granulation Tissue in Peri-Implant Osseous Defect: Case Series by Won-Bae Park, Jung-Min Ko, Ji-Young Han, Philip Kang

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Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation by Bo-Young Kim, Jung Min Ko, Mi-Hyun Park, Soo Kyung Koo

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A Korean boy with 46,XX testicular disorder of sex development caused by duplication by Gyung Min Lee, Jung Min Ko, Choong Ho Shin, Sei Won Yang

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Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome by Sanaa Choufani, Jung Min Ko, Youliang Lou, Cheryl Shuman, Leona Fishman, Rosanna Weksberg

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A Korean child diagnosed with malonic aciduria harboring a novel start codon mutation following presentation with dilated cardiomyopathy by Seung Hoon Lee, Jung Min Ko, Mi‐Kyoung Song, Junghan Song, Kyung Sun Park

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Clinical characteristics and effects of enzyme replacement therapy with elosulfase alfa in Korean patients with mucopolysaccharidosis type IVA by Seung Hoon Lee, Hwa Young Kim, Tae-Joon Cho, Hyoungmin Kim, Jung Min Ko

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Predictors of cervical myelopathy and hydrocephalus in young children with achondroplasia by Youngbo Shim, Jung Min Ko, Tae-Joon Cho, Seung‐Ki Kim, Ji Hoon Phi

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Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome by Naye Choi, Hwa Young Kim, Byung Chan Lim, Jong‐Hee Chae, Soo Yeon Kim, Jung Min Ko

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Growth patterns of young achondroplasia patients in Korea and predictability of neurosurgical procedures by Jong Seok Lee, Youngbo Shim, Tae-Joon Cho, Seung-Ki Kim, Jung Min Ko, Ji Hoon Phi

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A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing by Yoon-Myung Kim, Go Hun Seo, Gu-Hwan Kim, Jung Min Ko, Jin-Ho Choi, Han-Wook Yoo

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The natural history and prognostic factors of Graves' disease in Korean children and adolescents by Seung Min Song, Ji-Seok Youn, Jung Min Ko, Chong Kun Cheon, Jin-Ho Choi, Han Wook Yoo

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Prospective study of epigenetic alterations responsible for isolated hemihyperplasia/hemihypoplasia and their association with leg length discrepancy by Chang Ho Shin, Chaemoon Lim, Hwa Young Kim, Won Joon Yoo, Tae-Joon Cho, In Ho Choi, Jung Min Ko

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Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene by Ka Young Kim, You Joung Heo, Jung Min Ko, Young Ah Lee, Choong Ho Shin, Chang Seok Ki, Yun Jeong Lee

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