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Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
Endocrinology and Metabolism
2017 .01
Corrigendum: Table and Text Correction Recent Updates on Type 1 Diabetes Mellitus Management for Clinicians
Diabetes and Metabolism Journal
2018 .01
CORRIGENDUM
Women's Health Nursing
2018 .01
CORRIGENDUM: Correction of a Table of Contents in Section 5: Deep Learning in Medical Imaging
Neurospine
2020 .01
New, Novel Lipid-Lowering Agents for Reducing Cardiovascular Risk: Beyond Statins
Diabetes and Metabolism Journal
2022 .09
Association between Changes in Anthropometric Indices and in Fasting Insulin Levels among Healthy Korean Adolescents: The JS High School Study
Diabetes and Metabolism Journal
2022 .01
Younger-Onset Diabetes: Is the Age of Onset More Important than the Duration of Diabetes?
Endocrinology and Metabolism
2024 .02
Identification of LAMP2 mutations in early-onset hypertrophic cardiomyopathy by targeted exome sequencing
Journal of genetic medicine
2018 .01
Update on Monogenic Diabetes in Korea
Diabetes and Metabolism Journal
2020 .01
Corrigendum: 대학생의 코로나19 예방행위에 대한 영향요인
지역사회간호학회지
2022 .09
Genetic analysis using whole-exome sequencing in pediatric chronic kidney disease: a single center's experience
Childhood Kidney Diseases
2022 .06
Exome sequencing in a breast cancer family without BRCA mutation
Radiation oncology journal : ROJ
2015 .01
Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing
Annals of Dermatology
2017 .01
De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea
Clinical and Experimental Pediatrics
2019 .01
Comparison of Age of Onset and Frequency of Diabetic Complications in the Very Elderly Patients with Type 2 Diabetes
Endocrinology and Metabolism
2016 .01
CORRIGENDUM: CORRECTION OF TEXT. 진행성 갑상선암 환자에서 발생하는 Tyrosine Kinase Inhibitor의 이상반응
International Journal of Thyroidology
2019 .01
Utility of Clinical Exome Sequencing in Dystonia: A Single-Center Study From India
Journal Of Movement Disorders
2022 .05
Novel Pathogenic Variant (c.3178G>A) in the SMC1A Gene in a Family With Cornelia de Lange Syndrome Identified by Exome Sequencing
Annals of Laboratory Medicine
2015 .01
Corrigendum: Successful surgical missions for cleft
대한구강악안면외과학회지
2019 .01
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