Case Report: Whole genome sequencing identifies a novel deep intronic COL4A5 variant of uncertain significance in X-linked Alport syndrome by Hoon Seok Kim, Hoon Seok Kim, Myungshin Kim, Myungshin Kim, Jin-Soon Suh, Yeonhee Lee

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Hereditary renal hypouricemia with SLC22A12 mutation: A case report by Jisook Yim, Myungshin Kim, Jin-Soon Suh

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Tracing Emergence of SARS-CoV-2 Variants: Insights from Comprehensive Assessment Using Reverse Transcription Polymerase Chain Reaction and Whole Genome Sequencing by Duyeon Na, Yuna Hong, Chaeyeon Lee, Myungshin Kim

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Investigation of gut microbiota diversity according to infectious agent in pediatric infectious acute gastroenteritis in a Korean university hospital by You Ie Kim, Sang Yong Kim, Seungok Lee, Myungshin Kim, Woo Jin Kim

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The Clinically Significant Changes in the Composition and Functional Diversity of the Vaginal Microbiome in Women with Type 2 Diabetes Mellitus by Min Jeong Kim, Jaeeun Yoo, Soonjib Yoo, Mi Yeon Kwon, Seungok Lee, Myungshin Kim

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Machine-learning-based predictive classifier for bone marrow failure syndrome using complete blood count data by Jeongmin Seo, Chansub Lee, Youngil Koh, Choong Hyun Sun, Jong-Mi Lee, Hong Yul An, Myungshin Kim

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Diagnosis and Treatment of Pediatric Acute Megakaryoblastic Leukemia with NUP98::KDM5A Rearrangement: Case Report by Hyemin Kang, Suejung Jo, Jae Won Yoo, Seongkoo Kim, Jae Wook Lee, Nack-Gyun Chung, Bin Cho, Chae Yeon Lee, Myungshin Kim

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Inferior Outcomes of Fludarabine–Cyclophosphamide–Rituximab Chemotherapy in Korean Chronic Lymphocytic Leukemia Patients with Concurrent Thrombocytopenia and Anemia by Tong-Yoon Kim, Gi-June Min, Young-Woo Jeon, Seung-Ah Yahng, Seok-Goo Cho, Jong-Mi Lee, Myungshin Kim, Ki-Seong Eom

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Telomere Length and Genetic Variations in Acquired Pediatric Aplastic Anemia: A Flow-FISH Study in Korean Patients by Yuna Hong, Jong-Mi Lee, Chaeyeon Lee, Duyeon Na, Jin Jung, Ari Ahn, Jae Won Yoo, Jae Wook Lee, Nack-Gyun Chung, Myungshin Kim, Yonggoo Kim

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Tracing genomic instability in induced mesenchymal stromal cell manufacture: an integration-free transfection approach by Jong-Mi Lee, Chae Yeon Lee, Binna Seol, Chan Kwon Jung, Yonggoo Kim, Dain Kang, Haein Yu, Yuna Hong, Cho Lok Song, Yee Sook Cho, Myungshin Kim

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Poor prognostic implication of CDKN2 deletion in adult patients with Philadelphia chromosome-positive ALL by So Yeon Park, Daehun Kwag, Jin Jung, Gi June Min, Sung-Soo Park, Silvia Park, Sung-Eun Lee, Byung-Sik Cho, Ki-Seong Eom, Yoo-Jin Kim, Hee-Je Kim, Chang-Ki Min, Seok-Goo Cho, Yonggoo Kim, Myungshin Kim, Seok Lee, Jae-Ho Yoon

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P235: Exploring precision medicine through genome sequencing for patients suspected of rare genetic disorders by Soojin Hwang, Go Hun Seo, In Hee Choi, Seung-Woo Ryue, Jiyoung Oh, Yoo-Mi Kim, Baik-Lin Eun, Jung Hye Byeon, Eungu Kang, Myungshin Kim, Gu-Hwan Kim, Rin Khang, Jihye Kim, Kyoung Bo Kim, Jun Hong Park, Mi-Hyun Park, Beom Hee Lee, Hyun-Young Park

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Clinical implementation of a multidisciplinary pipeline for genome sequencing in rare diseases: A prospective, multicenter, observational cohort study by Soojin Hwang, Go Hun Seo, In Hee Choi, Seung‐Woo Ryue, Ji Young Oh, Yoo‐Mi Kim, Baik‐Lin Eun, Jung Hye Byeon, Eugu Kang, Myungshin Kim, Hoon Seok Kim, Soyoung Lee, Han Wool Kim, Dohyung Kim, Rin Khang, Jihye Kim, Dongseok Moon, Seokhui Jang, Yongjun Song, Gu‐Hwan Kim, Kyoung Bo Kim, Jun Hong Park, Seo Yeon Yang, Yoo Kyoung Choi, Su Min Ji, Oc‐Hee Kim, Mi‐Hyun Park, Hyun‐Young Park, Beom Hee Lee

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