Search research articles
Contact Us
Filters
Showing results (1-10 of 27) with videos related to
Page
of 3
Sort By:
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 26, 1998
Molecular and clinical characterization of Korean patients with congenital lipoid adrenal hyperplasia
H W Yoo, G H Kim
Journal of Korean Medical Science
|
June 4, 1998
Prenatal molecular evaluation of six fetuses in four unrelated Korean families with ornithine transcarbamylase deficiency
H W Yoo, G H Kim
AJNR. American Journal of Neuroradiology
|
May 5, 2001
Localized proton MR spectroscopy in infants with urea cycle defect
C G Choi, H W Yoo
Journal of Inherited Metabolic Disease
|
April 8, 2006
Two cases of citrullinaemia presenting with stroke
J H Choi, H Kim, H W Yoo
Journal of Medicinal Chemistry
|
November 21, 1998
Synthesis and cytotoxicity of 2-methyl-4, 9-dihydro-1-substituted-1H-imidazo[4,5-g]quinoxaline-4,9-diones and 2,3-disubstituted-5,10-pyrazino[2,3-g]quinoxalinediones
H W Yoo, M E Suh, S W Park
Journal of Korean Medical Science
|
February 1, 1993
Comparison of enzyme and DNA analysis in a Tay-Sachs disease carrier screening program
H W Yoo, K H Astrin, R J Desnick
Journal of Inherited Metabolic Disease
|
January 1, 1996
Identification of new mutations in the ornithine transcarbamylase (OTC) gene in Korean families
H W Yoo, G H Kim, D H Lee
Genomics
|
January 1, 1993
Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human gene
H W Yoo, C A Warner, C H Chen, et al.
Biological & Pharmaceutical Bulletin
|
March 22, 2000
Cytotoxic effects of pyridino[2,3-f]indole-4,9-diones on human tumor cell lines
M E Suh, H K Park, H W Yoo, et al.
The Journal of Clinical Investigation
|
February 1, 1992
Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene
C A Warner, H W Yoo, A G Roberts, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 26, 1998
Molecular and clinical characterization of Korean patients with congenital lipoid adrenal hyperplasia
H W Yoo, G H Kim
Journal of Korean Medical Science
|
June 4, 1998
Prenatal molecular evaluation of six fetuses in four unrelated Korean families with ornithine transcarbamylase deficiency
H W Yoo, G H Kim
AJNR. American Journal of Neuroradiology
|
May 5, 2001
Localized proton MR spectroscopy in infants with urea cycle defect
C G Choi, H W Yoo
Journal of Inherited Metabolic Disease
|
April 8, 2006
Two cases of citrullinaemia presenting with stroke
J H Choi, H Kim, H W Yoo
Journal of Medicinal Chemistry
|
November 21, 1998
Synthesis and cytotoxicity of 2-methyl-4, 9-dihydro-1-substituted-1H-imidazo[4,5-g]quinoxaline-4,9-diones and 2,3-disubstituted-5,10-pyrazino[2,3-g]quinoxalinediones
H W Yoo, M E Suh, S W Park
Journal of Korean Medical Science
|
February 1, 1993
Comparison of enzyme and DNA analysis in a Tay-Sachs disease carrier screening program
H W Yoo, K H Astrin, R J Desnick
Journal of Inherited Metabolic Disease
|
January 1, 1996
Identification of new mutations in the ornithine transcarbamylase (OTC) gene in Korean families
H W Yoo, G H Kim, D H Lee
Genomics
|
January 1, 1993
Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human gene
H W Yoo, C A Warner, C H Chen, et al.
Biological & Pharmaceutical Bulletin
|
March 22, 2000
Cytotoxic effects of pyridino[2,3-f]indole-4,9-diones on human tumor cell lines
M E Suh, H K Park, H W Yoo, et al.
The Journal of Clinical Investigation
|
February 1, 1992
Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene
C A Warner, H W Yoo, A G Roberts, et al.
Page
of 3