Browsing by Ajou Author

researcher image
김, 현주 Not currently indexed
[School of Medicine / Graduate School of Medicine] - [Medical Genetics]

Author IDs

ORCID
-
WOS
-
SCOPUS
-

Showing results 41 to 54 of 54

This table browses all dspace content
Pub YearTitleAuthor(s)
2007A Case of Familial Multiple Endocrine Neoplasia Type 1 with MEN1 Gene Mutation.김대중, 김현주, 김혜진, 이관우, 정선용, 정윤석
200716q-linked autosomal dominant cerebellar ataxia in a Korean family.김현주, 이필휴, 정선용
2006Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.김현주
2006Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.김현주, 박상진, 정선용
2006The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.김현주, 박상진, 정선용
2005Childhood X-linked adrenoleukodystrophy: clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up.김현주
2004Novel and recurrent mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia.김현주
2004Expression and secretion of human glucocerebrosidase mediated by recombinant lentivirus vectors in vitro and in vivo: implications for gene therapy of Gaucher disease.김현주
2004Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis.김선용, 김현주, 방오영, 이필휴, 허균
2003Clinical and neuroradiological features of patients with spinocerebellar ataxias from Korean kindreds.김현주, 방오영, 이필휴, 허균
2001Diagnostic patterns of very-long-chain fatty acids in plasma of patients with X-linked adrenoleukodystrophy.김현주
2000Assignment of the kinesin family member 4 genes (KIF4A and KIF4B) to human chromosome bands Xq13.1 and 5q33.1 by in situ hybridization.김완기, 김현주, 이영미, 하만준
1999Hepatopulmonary syndrome in Gaucher disease with right-to-left shunt: evaluation and measurement using Tc-99m MAA.김현주, 박찬희, 한명호
1998Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation.김현주
1 2 3

Browse