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U K Kim

Showing results (11-20 of 26) with videos related to

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Clinical Genetics|May 15, 2009
Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implantsH-K Lee, S-H Lee, K-Y Lee, et al.
International Journal of Pediatric Otorhinolaryngology|July 1, 2008
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patientsK Y Lee, S Y Choi, J W Bae, et al.
Clinical Genetics|May 8, 2010
The Trp117Arg mutation of the COCH gene causes deafness in KoreansJ-I Baek, H-J Cho, S-J Choi, et al.
Human Heredity|August 7, 1999
Allelic frequencies of six (CA)n microsatellite markers of the dystrophin gene in the Korean populationU K Kim, M S Cho, J J Chae, et al.
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|September 20, 2017
Expression patterns of members of the isocitrate dehydrogenase gene family in murine inner earY-R Kim, K-H Kim, S Lee, et al.
Human Biology|May 3, 2001
Polymorphic DNA haplotypes at the human low-density lipoprotein receptor gene locus in KoreansJ J Chae, S H Kim, U K Kim, et al.
Clinical Chemistry|September 3, 1999
Long-distance PCR-based screening for large rearrangements of the LDL receptor gene in Korean patients with familial hypercholesterolemiaS H Kim, J H Bae, J J Chae, et al.
Clinical Genetics|July 28, 1999
Three novel small deletion mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemiaJ J Chae, S H Kim, U K Kim, et al.
Clinical Genetics|April 27, 2000
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemiaJ A Shin, S H Kim, U K Kim, et al.
Molecular and Cellular Probes|June 17, 1999
Polymorphisms in the human autosomal dominant polycystic kidney disease 2 (PKD2) geneU K Kim, J H Shin, K B Lee, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Clinical Genetics|May 15, 2009
Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implantsH-K Lee, S-H Lee, K-Y Lee, et al.
International Journal of Pediatric Otorhinolaryngology|July 1, 2008
Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patientsK Y Lee, S Y Choi, J W Bae, et al.
Clinical Genetics|May 8, 2010
The Trp117Arg mutation of the COCH gene causes deafness in KoreansJ-I Baek, H-J Cho, S-J Choi, et al.
Human Heredity|August 7, 1999
Allelic frequencies of six (CA)n microsatellite markers of the dystrophin gene in the Korean populationU K Kim, M S Cho, J J Chae, et al.
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|September 20, 2017
Expression patterns of members of the isocitrate dehydrogenase gene family in murine inner earY-R Kim, K-H Kim, S Lee, et al.
Human Biology|May 3, 2001
Polymorphic DNA haplotypes at the human low-density lipoprotein receptor gene locus in KoreansJ J Chae, S H Kim, U K Kim, et al.
Clinical Chemistry|September 3, 1999
Long-distance PCR-based screening for large rearrangements of the LDL receptor gene in Korean patients with familial hypercholesterolemiaS H Kim, J H Bae, J J Chae, et al.
Clinical Genetics|July 28, 1999
Three novel small deletion mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemiaJ J Chae, S H Kim, U K Kim, et al.
Clinical Genetics|April 27, 2000
Identification of four novel mutations of the low-density lipoprotein receptor gene in Korean patients with familial hypercholesterolemiaJ A Shin, S H Kim, U K Kim, et al.
Molecular and Cellular Probes|June 17, 1999
Polymorphisms in the human autosomal dominant polycystic kidney disease 2 (PKD2) geneU K Kim, J H Shin, K B Lee, et al.
Pageof 3