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Kabuki syndrome: clinical and molecular characteristics.
Cheon CK, Ko JM. Cheon CK, et al. Korean J Pediatr. 2015 Sep;58(9):317-24. doi: 10.3345/kjp.2015.58.9.317. Epub 2015 Sep 21. Korean J Pediatr. 2015. PMID: 26512256 Free PMC article. Review.
Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.
Seo GH, Lee H, Lee J, Han H, Cho YK, Kim M, Choi Y, Choi J, Choi IH, Rhie S, Chae KY, Kim YM, Cheon CK, Kim SJ, Lee J, Kang E, Byeon JH, Yu HJ, Shin YL, Oh A, Kim WJ, Yum MS, Lee BH, Eun BL. Seo GH, et al. Among authors: cheon ck. Mol Med. 2022 Mar 26;28(1):38. doi: 10.1186/s10020-022-00464-x. Mol Med. 2022. PMID: 35346031 Free PMC article.
Evaluation of users' level of satisfaction for an artificial intelligence-based diagnostic program in pediatric rare genetic diseases.
Choi IH, Seo GH, Park J, Kim YM, Cheon CK, Kim YM, Oh A, Byeon JH, Kang E, Shin YL, Lee JE, Kim SJ, Yu HJ, Kim WJ, Choi BY, Kim BJ, Kim YH, Im GJ, Lee HJ, Kim HJ, Han SH, Lee BH, Eun BL. Choi IH, et al. Among authors: cheon ck. Medicine (Baltimore). 2022 Jul 15;101(28):e29424. doi: 10.1097/MD.0000000000029424. Medicine (Baltimore). 2022. PMID: 35838999 Free PMC article.
Clinical and molecular spectra of BRAF-associated RASopathy.
Lee Y, Choi Y, Seo GH, Kim GH, Choi IH, Keum C, Ko JM, Cheon CK, Jeon J, Choi JH, Yoo HW, Lee BH. Lee Y, et al. Among authors: cheon ck. J Hum Genet. 2021 Apr;66(4):389-399. doi: 10.1038/s10038-020-00852-3. Epub 2020 Oct 10. J Hum Genet. 2021. PMID: 33040082
Low prevalence of classical galactosemia in Korean population.
Lee BH, Cheon CK, Kim JM, Kang M, Kim JH, Yang SH, Kim GH, Choi JH, Yoo HW. Lee BH, et al. Among authors: cheon ck. J Hum Genet. 2011 Jan;56(1):94-6. doi: 10.1038/jhg.2010.152. Epub 2010 Dec 9. J Hum Genet. 2011. PMID: 21150919
73 results