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Human Mutation|January 1, 1995
Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1S H Hahn, D Krasnewich, M Brantly, et al.The Laryngoscope|September 13, 2000
Connexin26 mutations associated with nonsyndromic hearing lossH J Park, S H Hahn, Y M Chun, et al.Biochemical and Biophysical Research Communications|May 21, 1999
Cloning and characterization of the promoter region of the Wilson disease geneW J Oh, E K Kim, K D Park, et al.Cell|February 1, 1981
The identification of calmodulin-binding sites on mitochondria in cultured 3T3 cellsR L Pardue, M A Kaetzel, S H Hahn, et al.Molecular Genetics and Metabolism|January 27, 2005
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type IS Tortorelli, S H Hahn, T M Cowan, et al.The Review of Scientific Instruments|December 3, 2008
Magnetic diagnostics for the first plasma operation in Korea Superconducting Tokamak Advanced ResearchS G Lee, J G Bak, E M Ka, et al.Journal of Medical Genetics|July 25, 1998
Extensive form of aplasia cutis congenita: a new syndrome?M S Park, S H Hahn, C H Hong, et al.American Journal of Dentistry|November 9, 2001
Color stability of glass-ionomers and polyacid-modified resin-based composites in various environmental solutionsB S Lim, H J Moon, K W Baek, et al.Orthopedics|October 1, 1991
A clinical study of stress fractures in sports activitiesK I Ha, S H Hahn, M Y Chung, et al.Pediatric Research|February 1, 1994
Metallothionein synthesis and degradation in Indian childhood cirrhosis fibroblastsS H Hahn, M L Brantly, C Oliver, et al.Pageof 4