Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Gu-Hwan Kim

Showing results (11-20 of 173) with videos related to

Pageof 18
Sort By:
The Journal of Craniofacial Surgery|January 31, 2018
Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma SyndromeYookyeong Carolyn Sim, Gu-Hwan Kim, Sung-Weon Choi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 17, 2005
Comparison of clinical, radiological and molecular findings in Korean infants and children with achondroplasia and hypochondroplasiaYoung-Lim Shin, Jin-Ho Choi, Gu-Hwan Kim, et al.
European Journal of Pediatrics|October 15, 2008
A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase geneJung Min Ko, Chong-Kun Cheon, Gu-Hwan Kim, et al.
Journal of Human Genetics|November 21, 2008
PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndromeJung Min Ko, Jae-Min Kim, Gu-Hwan Kim, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2020
Molecular Characteristics of Sequence Variants in GATA4 in Patients with 46,XY Disorders of Sex Development without Cardiac DefectsJin-Ho Choi, Yena Lee, Arum Oh, et al.
The Journal of Molecular Diagnostics : JMD|February 19, 2026
High-yield DNA-based neurofibromatosis type 1 diagnostics reveals population-specific mutation landscape in 1,917 KoreansJaeryuk Kim, Gu-Hwan Kim, Soojin Hwang, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 3, 2020
Functional Characteristics of Novel FGFR1 Mutations in Patients with Isolated Gonadotropin-Releasing Hormone DeficiencyJin-Ho Choi, Arum Oh, Yena Lee, et al.
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasiaHye Won Park, Byung Ok Kwak, Gu-Hwan Kim, et al.
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndromeJi Won Koh, So Young Kang, Gu Hwan Kim, et al.
Medicine|March 13, 2026
Caregiver quality of life and burden in rare genetic diseases in South KoreaSunyoung Choi, Ja Hye Kim, Gu-Hwan Kim, et al.
Pageof 18

Showing results (11-20 of 173) with videos related to

Sort By:
Pageof 18
The Journal of Craniofacial Surgery|January 31, 2018
Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma SyndromeYookyeong Carolyn Sim, Gu-Hwan Kim, Sung-Weon Choi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 17, 2005
Comparison of clinical, radiological and molecular findings in Korean infants and children with achondroplasia and hypochondroplasiaYoung-Lim Shin, Jin-Ho Choi, Gu-Hwan Kim, et al.
European Journal of Pediatrics|October 15, 2008
A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase geneJung Min Ko, Chong-Kun Cheon, Gu-Hwan Kim, et al.
Journal of Human Genetics|November 21, 2008
PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndromeJung Min Ko, Jae-Min Kim, Gu-Hwan Kim, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2020
Molecular Characteristics of Sequence Variants in GATA4 in Patients with 46,XY Disorders of Sex Development without Cardiac DefectsJin-Ho Choi, Yena Lee, Arum Oh, et al.
The Journal of Molecular Diagnostics : JMD|February 19, 2026
High-yield DNA-based neurofibromatosis type 1 diagnostics reveals population-specific mutation landscape in 1,917 KoreansJaeryuk Kim, Gu-Hwan Kim, Soojin Hwang, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 3, 2020
Functional Characteristics of Novel FGFR1 Mutations in Patients with Isolated Gonadotropin-Releasing Hormone DeficiencyJin-Ho Choi, Arum Oh, Yena Lee, et al.
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
p.R182C mutation in Korean twin with congenital lipoid adrenal hyperplasiaHye Won Park, Byung Ok Kwak, Gu-Hwan Kim, et al.
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
Central precocious puberty in a patient with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndromeJi Won Koh, So Young Kang, Gu Hwan Kim, et al.
Medicine|March 13, 2026
Caregiver quality of life and burden in rare genetic diseases in South KoreaSunyoung Choi, Ja Hye Kim, Gu-Hwan Kim, et al.
Pageof 18