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Gu-Hwan Kim

Showing results (21-30 of 173) with videos related to

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Journal of Korean Medical Science|October 29, 2008
Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosisJung Min Ko, Gu-Hwan Kim, Kyung Mo Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Long-term clinical course of a patient with mucopolysaccharidosis type IIIBJa Hye Kim, Yang Hyun Chi, Gu-Hwan Kim, et al.
Pediatric Neurology|February 12, 2011
Argininemia presenting with progressive spastic diplegiaBeom Hee Lee, Hye Young Jin, Gu-Hwan Kim, et al.
Korean Journal of Pediatrics|July 9, 2011
Testicular adrenal rest tumors in a patient with untreated congenital adrenal hyperplasiaHye Young Jin, Jin Ho Choi, Gu Hwan Kim, et al.
Clinical Endocrinology|February 13, 2010
Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndromeJung Min Ko, Jae-Min Kim, Gu-Hwan Kim, et al.
Pediatric Cardiology|August 25, 2016
Cardiac Manifestations and Associations with Gene Mutations in Patients Diagnosed with RASopathiesWon Kyoung Jhang, Jin-Ho Choi, Beom Hee Lee, et al.
Cardiology in the Young|September 13, 2014
Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestationsWon Kyoung Jhang, Beom Hee Lee, Gu-Hwan Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Compound heterozygous mutations of <i>ACADS</i> gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures reviewSe Jin An, Sook Za Kim, Gu Hwan Kim, et al.
Fertility and Sterility|February 28, 2006
A novel frameshift mutation in the 5alpha-reductase type 2 gene in Korean sisters with male pseudohermaphroditismSung Hoon Kim, Kun Suk Kim, Gu Hwan Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milkKyung Lae Cho, Yeo Jin Kim, Song Hyun Yang, et al.
Pageof 18

Showing results (21-30 of 173) with videos related to

Sort By:
Pageof 18
Journal of Korean Medical Science|October 29, 2008
Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosisJung Min Ko, Gu-Hwan Kim, Kyung Mo Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Long-term clinical course of a patient with mucopolysaccharidosis type IIIBJa Hye Kim, Yang Hyun Chi, Gu-Hwan Kim, et al.
Pediatric Neurology|February 12, 2011
Argininemia presenting with progressive spastic diplegiaBeom Hee Lee, Hye Young Jin, Gu-Hwan Kim, et al.
Korean Journal of Pediatrics|July 9, 2011
Testicular adrenal rest tumors in a patient with untreated congenital adrenal hyperplasiaHye Young Jin, Jin Ho Choi, Gu Hwan Kim, et al.
Clinical Endocrinology|February 13, 2010
Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndromeJung Min Ko, Jae-Min Kim, Gu-Hwan Kim, et al.
Pediatric Cardiology|August 25, 2016
Cardiac Manifestations and Associations with Gene Mutations in Patients Diagnosed with RASopathiesWon Kyoung Jhang, Jin-Ho Choi, Beom Hee Lee, et al.
Cardiology in the Young|September 13, 2014
Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestationsWon Kyoung Jhang, Beom Hee Lee, Gu-Hwan Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Compound heterozygous mutations of <i>ACADS</i> gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures reviewSe Jin An, Sook Za Kim, Gu Hwan Kim, et al.
Fertility and Sterility|February 28, 2006
A novel frameshift mutation in the 5alpha-reductase type 2 gene in Korean sisters with male pseudohermaphroditismSung Hoon Kim, Kun Suk Kim, Gu Hwan Kim, et al.
Korean Journal of Pediatrics|December 27, 2016
Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milkKyung Lae Cho, Yeo Jin Kim, Song Hyun Yang, et al.
Pageof 18