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Showing results 221 to 227 of 227

Pub YearTitleAJOU Author(s)
2011Two Children with Saethre-Chotzen Syndrome Confirmed by the TWIST1 Gene Analysis윤수한, 정선용
2012Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence손영배
2010Type 2 Diabetes Genetic Association Database manually curated for the study design and odds ratio.진현석
2023UBAP2 plays a role in bone homeostasis through the regulation of osteoblastogenesis and osteoclastogenesis김범택, 김정현, 박은국, 원예연, 정선용, 정윤석, 최용준
2022Updates on Paget’s Disease of Bone손영배, 정윤석, 최용준
2023Using low-dose octreotide with diazoxide-resistant congenital hyperinsulinism resulting from com-pound heterozygous mutations in the ABCC8 gene손영배, 이해상, 황진순
2015VE1 antibody is not highly specific for the BRAF V600E mutation in thyroid cytology categories with the exception of malignant cases.김대중, 김장희, 소의영, 신승수, 이기범, 이정훈, 임현이, 정선용, 정윤석, 한재호
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