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Genetic-pathologic characterization of myeloproliferative neoplasms.
Kim Y, Park J, Jo I, Lee GD, Kim J, Kwon A, Choi H, Jang W, Chae H, Han K, Eom KS, Cho BS, Lee SE, Yang J, Shin SH, Kim H, Ko YH, Park H, Jin JY, Lee S, Jekarl DW, Yahng SA, Kim M. Kim Y, et al. Among authors: choi h. Exp Mol Med. 2016 Jul 22;48(7):e247. doi: 10.1038/emm.2016.55. Exp Mol Med. 2016. PMID: 27444979 Free PMC article.
Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea.
Jang W, Kim Y, Han E, Park J, Chae H, Kwon A, Choi H, Kim J, Son JO, Lee SJ, Hong BY, Jang DH, Han JY, Lee JH, Kim SY, Lee IG, Sung IK, Moon Y, Kim M, Park JH. Jang W, et al. Among authors: choi h. Ann Lab Med. 2019 May;39(3):299-310. doi: 10.3343/alm.2019.39.3.299. Ann Lab Med. 2019. PMID: 30623622 Free PMC article.
A Mutation in ZNF143 as a Novel Candidate Gene for Endothelial Corneal Dystrophy.
Kim Y, You HJ, Park SH, Kim MS, Chae H, Park J, Jekarl DW, Kim J, Kwon A, Choi H, Kim Y, Paek AR, Lee A, Kim JM, Park SY, Kim Y, Joo K, Jung J, Chung SH, Mok JW, Kim M. Kim Y, et al. Among authors: choi h. J Clin Med. 2019 Aug 6;8(8):1174. doi: 10.3390/jcm8081174. J Clin Med. 2019. PMID: 31390831 Free PMC article.
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