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    Neutralizing Antibodies and Cytokines in Breast Milk After Coronavirus Disease 2019 (COVID-19) mRNA Vaccination.Obstetrics & Gynecology: November 30, 2021 - Volume - Issue - 10.1097/AOG.0000000000004661 doi: 10.1097/AOG.0000000000004661

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    Association of Human Milk Antibody Induction, Persistence, and Neutralizing Capacity With SARS-CoV-2 Infection vs mRNA Vaccination.JAMA Pediatr. Published online November 10, 2021. doi:10.1001/jamapediatrics.2021.4897

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    Optimized Detoxification of a Live Attenuated Vaccine Strain (SG9R) to Improve Vaccine Strategy against Fowl TyphoidVaccines (Basel) . 2021 Feb 3;9(2):122. doi: 10.3390/vaccines9020122.

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    Molecular evolution of Salmonella enterica subsp. enterica serovar Gallinarum biovar Gallinarum in the fieldVet Microbiol . 2019 Aug;235:63-70. doi: 10.1016/j.vetmic.2019.05.019. Epub 2019 May 24.

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    Chaenomelis fructus inhibits osteoclast differentiation by suppressing NFATc1 expression and prevents ovariectomy-induced osteoporosisBMC Complement Med Ther . 2020 Feb 5;20(1):35. doi: 10.1186/s12906-020-2841-9.

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    Comparison of five membrane filters to collect bioaerosols for airborne microbiome analysisJ Appl Microbiol . 2020 Dec 17. doi: 10.1111/jam.14972. Online ahead of print.

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    Case of the Index Patient Who Caused Tertiary Transmission of COVID-19 Infection in Korea: the Application of Lopinavir/Ritonavir for the Treatment of COVID-19 Infected Pneumonia Monitored by Quantitative RT-PCR.J Korean Med Sci. 2020 Feb 17;35(6):e79.

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    Array Comparative Genomic Hybridization as the First-line Investigation for Neonates with Congenital Heart Disease: Experience in a Single Tertiary Center.Korean Circ J. 2018 Mar;48(3):209-216

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    A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.Clin Exp Reprod Med. 2014 Dec;41(4):168-73

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    Pre-implantation genetic diagnosis and pre-implantation genetic screening: two years experience at a single center.Obstet Gynecol Sci. 2018 Jan;61(1):95-101

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    Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization.J Korean Med Sci. 2016 Aug;31(8):1307-18

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    Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center study.Yonsei Med J. 2013 Nov;54(6):1463-70

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    Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.Ann Clin Lab Sci. 2013 Summer;43(3):332-6

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    Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH.J Genet Med. 2013 Jun;10(1):52-56

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    Comprehensive chromosome analysis of blastocysts before implantation using array CGH.Mol Cytogenet. 2013 Jun 3;6(1):22

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    The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns.Mol Cytogenet. 2013 Jun 1;6(1):21

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    22q11.2 Microduplication with thyroid hemiagenesis.Horm Res Paediatr. 2013;79(4):243-9

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    Reciprocal deletion and duplication of 17p11.2-11.2: Korean patients with Smith-Magenis syndrome and Potocki-Lupski syndrome.J Korean Med Sci. 2012 Dec;27(12):1586-90

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    Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.J Hum Genet. 2013 Feb;58(2):73-7

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    Clinical and cytogenetic features of a Potocki-Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1.Brain Dev. 2013 Aug;35(7):681-5

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    14q32.33 Deletion Identified by array-CGH in a 5-year old-girl with Seizure.J Genet Med. 2011 Jun;8(1):62-66

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    Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.Mol Cytogenet. 2011 May 9;4:12

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    Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.J Korean Med Sci. 2010 Dec;25(12):1798-801

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    Clinical and genetic characteristics of Korean patients with Gaucher disease.Blood Cells Mol Dis. 2011 Jan 15;46(1):11-4

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    Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis Type 1J Kor Med Sci, 2010 Feb;25:804-808

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    The spectrum of 5p deletion in Korean 20 patients with Cri du chat syndrome.J Genet Med. 2007 Dec;4(2):133-141

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