Association of ATP7BMutation Detection Rate with Biochemical Characteristics in Korean Patients with Wilson DiseasePARK, Hyung-Doo; PARK, Hyun-Kyung; CHUNG, Hae-Sun et al.Annals of clinical and laboratory science. 2010, Vol 40, Num 1, pp 15-25, issn 0091-7370, 11 p.Article

Clinical and Genetic Analysis of Korean Patients with Cornelia de Lange Syndrome: Two Novel NIPBL MutationsPARK, Hyung-Doo; KI, Chang-Seok; KIM, Jong-Won et al.Annals of clinical and laboratory science. 2010, Vol 40, Num 1, pp 20-25, issn 0091-7370, 6 p.Article

A novel PHKA2 gross deletion mutation in a Korean patient with X-linked liver glycogenosis type IPARK, Kyoung-Jin; PARK, Hyung-Doo; LEE, Soo-Youn et al.Annals of clinical and laboratory science. 2011, Vol 41, Num 2, pp 197-200, issn 0091-7370, 4 p.Article

Associations between CYP2E1 promoter polymorphisms and plasma 1,3-dimethyluric acid/theophylline ratiosYOON, Yeomin; PARK, Hyung-Doo; KYOUNG UN PARK et al.European journal of clinical pharmacology. 2006, Vol 62, Num 8, pp 627-631, issn 0031-6970, 5 p.Article

Follicle-stimulating hormone (FSH), current suicidal ideation and attempt in female patients with major depressive disorderBORA KIM; KANG, Eun-Suk; FAVA, Maurizio et al.Psychiatry research (Print). 2013, Vol 210, Num 3, pp 951-956, issn 0165-1781, 6 p.Article

Biochemical and molecular investigation of two Korean patients with glycogen storage disease type IIIOH, Sue-Hyun; PARK, Hyung-Doo; KI, Chang-Seok et al.Clinical chemistry and laboratory medicine. 2008, Vol 46, Num 9, pp 1245-1249, issn 1434-6621, 5 p.Article

Multiplex Enzyme Assay for Galactosemia Using Ultraperformance Liquid Chromatography―Tandem Mass SpectrometryKO, Dae-Hyun; JUN, Sun-Hee; PARK, Hyung-Doo et al.Clinical chemistry (Baltimore, Md.). 2010, Vol 56, Num 5, pp 764-771, issn 0009-9147, 8 p.Article

Clinical, Biochemical, and Genetic Analysis of Two Korean Patients with Trichorhinophalangeal Syndrome Type I and Growth Hormone DeficiencyYOUNG BAE SOHN; KI, Chang-Seok; SUNG WON PARK et al.Annals of clinical and laboratory science. 2012, Vol 42, Num 3, pp 307-312, issn 0091-7370, 6 p.Article

SLC22A5 Mutations in a Patient with Systemic Primary Carnitine Deficiency: The First Korean Case Confirmed by Biochemical and Molecular InvestigationYOUNG AHN YOON; DONG HWAN LEE; KI, Chang-Seok et al.Annals of clinical and laboratory science. 2012, Vol 42, Num 4, pp 424-428, issn 0091-7370, 5 p.Article

Clinical, biochemical, and genetic analysis of a Korean neonate with hereditary tyrosinemia type 1PARK, Hyung-Doo; DONG HWAN LEE; CHOI, Tae-Youn et al.Clinical chemistry and laboratory medicine. 2009, Vol 47, Num 8, pp 930-933, issn 1434-6621, 4 p.Article

Multiplex Ligation-Dependent Probe Amplification Assay for Diagnosis of Congenital Adrenal HyperplasiaJANG, Ja-Hyun; JIN, Dong-Kyu; KIM, Jong-Hwa et al.Annals of clinical and laboratory science. 2011, Vol 41, Num 1, pp 44-47, issn 0091-7370, 4 p.Article

Mutations of ACADS Gene Associated with Short-Chain Acyl-Coenzyme A Dehydrogenase DeficiencySE HWA KIM; PARK, Hyung-Doo; YEAU, Sunghee et al.Annals of clinical and laboratory science. 2011, Vol 41, Num 1, pp 84-88, issn 0091-7370, 5 p.Article

Three Korean Patients with Maple Syrup Urine Disease: Four Novel Mutations in the BCKDHA GenePARK, Hyung-Doo; DONG HWAN LEE; YONG HEE HONG et al.Annals of clinical and laboratory science. 2011, Vol 41, Num 2, pp 167-173, issn 0091-7370, 7 p.Article

Real-time multiplex PCR assay for genotyping of three apolipoprotein E alleles and two choline acetyltransferase alleles with three hybridization probesPARK, Hyung-Doo; KYOUNG UN PARK; KIM, Ki-Woong et al.Clinical chemistry and laboratory medicine. 2007, Vol 45, Num 3, pp 346-350, issn 1434-6621, 5 p.Article