Showing results 1 to 7 of 7
Issue Date | Title | Author(s) | Type |
---|---|---|---|
2015 | Atypical hemolytic uremic syndrome: Korean pediatric series | 이승주 | Article |
2004 | Charcot-Marie-Tooth 환자에서 GJB1, EGR2, NEFL 유전자 돌연변이 및 임상적, 전기생리학적, 병리학적 특성 분석 | 趙賢智 | Master's Thesis |
2017 | Novel deletion mutation of HLA-B*40:02 gene in acquired aplastic anemia | 허정원; 문영철; 정혜선; 정태동 | Article |
2018 | PSEN1 p. Thr116Ile Variant in Two Korean Families with Young Onset Alzheimer's Disease | 정지향 | Article |
2017 | Simultaneous Profiling of DNA Mutation and Methylation by Melting Analysis Using Magnetoresistive Biosensor Array | 이정록 | Article |
2019 | Somatic mutation of HLA-DRB1*04:03 in a patient with myelodysplastic syndrome at diagnosis | 허정원; 문영철; 정태동; 박설희 | Article |
2005 | Two novel mutations in the aquaporin 2 gene in a girl with congenital nephrogenic diabetes insipidus | 조수진 | Article |