A loss function approach to group preference aggregation in the AHP von Cho, Yong-Gon, Cho, Keun-Tae

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A novel variant of the POLR3A gene in a patient with hypomyelinating POLR3-related leukodystrophy von Yoon Han, Ji, Gon Cho, Yong, Park, Joonhong, Jang, Woori

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Diversity of Clinical and Molecular Characteristics in Korean Patients with 16p11.2 Microdeletion Syndrome von Han, Ji Yoon, Cho, Yong Gon, Jo, Dae Sun, Park, Joonhong

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Clinical and Genetic Characteristics of Early and Advanced Gastric Cancer von Ha, Gi Won, Hwang, Hong Pil, Cho, Yong Gon, Park, Joonhong

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Isolation of EpCAM+/CD133− hepatic progenitor cells von Hao, P.P., Medical School and Hospital, Jeonju, Republic of Korea, Lee, M.J., Medical School and Hospital, Jeonju, Republic of Korea, Yu, G.R., Medical School and Hospital, Jeonju, Republic of Korea, Kim, I.H., Medical School and Hospital, Jeonju, Republic of Korea, Cho, Y.G., Chonbuk National University Medical School and Hospital, Jeonju, Republic of Korea, Kim, D.G., Medical School and Hospital, Jeonju, Republic of Korea

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Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis von Yun, Seok-Kweon, Cho, Yong-Gon, Song, Ki Hun, Hwang, Su-Ran, Kim Yoon, Sung-Joo, Choi, Keon-Woo, Kim, Han-Uk, Park, Jin

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Accuracy Validation of the Elecsys HBsAg II Quant Assay and Its Utility in Resolving Equivocal Qualitative HBsAg Results von Lee, Jaehyeon, Lee, Seung Yeob, Cho, Yong Gon, Kim, Dal Sik, Park, Joonhong

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Isolation and Genetic Characterization of Orientia tsutsugamushi from Scrub Typhus Patients in Gyeongsangnam-do, Korea von Ha, Jong-Hun, Lee, Dong-Hae, Park, Jin-Sik, Cho, Oh Hyun, Kim, Dong-Hoon, Ha, Na-Young, Cho, Nam-Hyuck, Hwang, Kyu Jam, Cho, Yong-Gon, Lee, Hye-Soo, Lee, Won Kil, Lee, Yoo Chul, Cho, Myung-Je, Lee, Woo-Kon, Shin, Min-Kyoung

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Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report von Park, Joonhong, Yhim, Ho-Young, Kang, Kyung Pyo, Bae, Tae Won, Cho, Yong Gon

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A NOVEL C.800G>C VARIANT OF THE ITM2B GENE IN FAMILIAL KOREAN DEMENTIA von Rhyu, Jee-Min, Park, Joonhong, Shin, Byoung-Soo, Cho, Yong Gon, Kim, Ko Woon

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Clinical Features and Risk Factors Associated With 30-Day Mortality in Patients With Pneumonia Caused by Hypervirulent Klebsiella pneumoniae (hvKP) von Hwang, Jeong-Hwan, Handigund, Mallikarjun, Hwang, Joo-Hee, Cho, Yong Gon, Kim, Dal Sik, Lee, Jaehyeon

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The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure von Kim, Soo Yeon, Lee, Seungbok, Woo, Hyewon, Han, Jiyeon, Ko, Young Jun, Shim, Youngkyu, Park, Soojin, Jang, Se Song, Lim, Byung Chan, Ko, Jung Min, Kim, Ki Joong, Cho, Anna, Kim, Hunmin, Hwang, Hee, Choi, Ji Eun, Kim, Man Jin, Moon, Jangsup, Seong, Moon-Woo, Park, Sung Sup, Choi, Sun Ah, Lee, Ji Eun, Kwon, Young Se, Sohn, Young Bae, Kim, Jon Soo, Kim, Won Seop, Lee, Yun Jeong, Kwon, Soonhak, Kim, Young Ok, Kook, Hoon, Cho, Yong Gon, Cheon, Chong Kun, Kang, Ki-Soo, Song, Mi-Ryoung, Kim, Young-Joon, Cha, Hyuk-Jin, Choi, Hee-Jung, Kee, Yun, Park, Sung-Gyoo, Baek, Seung Tae, Choi, Murim, Ryu, Dong-Sung, Chae, Jong-Hee

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Case Report: Novel Likely Pathogenic ACTN2 Variant Causing Heterogeneous Phenotype in a Korean Family With Left Ventricular Non-compaction von Park, Joonhong, Cho, Yong Gon, Park, Ha Wook, Cho, Jung Sun

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Case report: Compound heterozygosity in PKLR gene with a large exon deletion and a novel rare p.Gly536Asp variant as a cause of severe pyruvate kinase deficiency von Kim, Minsun, Lee, Seung Yeob, Kim, Namsu, Lee, Jaehyeon, Kim, Dal Sik, Park, Joonhong, Cho, Yong Gon

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Dermabacter jinjuensis sp. nov., a novel species of the genus Dermabacter isolated from a clinical specimen von Park, Young Kyoung, Lee, Kyeong Min, Lee, Woo-Kon, Cho, Myung-Je, Lee, Hye-Soo, Cho, Yong-Gon, Lee, Yoo Chul, Lee, Won Kil, Seong, Won Keun, Hwang, Kyu Jam

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Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study von Kwak, Byung Ok, Kwon, Young Se, Hong, Young Jin, Nahm, Chung Hyun, Jang, Woori, Uh, Young, Cho, Yong Gon, Kim, Jimyung, Kim, Myungshin, Kim, Dong Hyun

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A case of torsion of a mucinous cystadenoma in triple-X syndrome with pure gonadal dysgenesis von Lee, Jeong-Heon, Kim, Kwan-Sik, Cho, Yong-Gon

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SPA0355 prevents ovariectomy-induced bone loss in mice von Kim, Sang Hoon, Zhang, Zhongkai, Moon, Young Jae, Park, Il Woon, Cho, Yong Gon, Jeon, Raok, Park, Byung-Hyun

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MYC rearrangement involving a novel non-immunoglobulin chromosomal locus in precursor B-cell acute lymphoblastic leukemia von Seo, Ja-Young, Lee, Soo Hyun, Kim, Hee-Jin, Yoo, Keon Hee, Koo, Hong Hoe, Cho, Yong Gon, Choi, Sam Im, Kim, Sun-Hee

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A double mutation of the ryanodine receptor type 1 gene in a malignant hyperthermia family with multiminicore myopathy von Jeong, Seul-Ki, Kim, Dong-Chan, Cho, Yong-Gon, Sunwoo, Il-Nam, Kim, Dal-Sik

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