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Jung Min Ko

Showing results (1-10 of 166) with videos related to

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Journal of Korean Neurosurgical Society|May 27, 2016
Genetic Syndromes Associated with CraniosynostosisJung Min Ko
Korean Circulation Journal|September 29, 2015
Genetic Syndromes associated with Congenital Heart DiseaseJung Min Ko
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
Genetic syndromes associated with overgrowth in childhoodJung Min Ko
Korean Circulation Journal|March 21, 2018
Chromosomal Microarray: Application for Congenital Heart DiseasesJung Min Ko
Clinical and Experimental Pediatrics|November 21, 2023
Advancing orphan drug development for rare diseasesJung Min Ko
Korean Journal of Pediatrics|October 30, 2015
Kabuki syndrome: clinical and molecular characteristicsChong-Kun Cheon, Jung Min Ko
Annals of Pediatric Endocrinology & Metabolism|July 6, 2022
Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhoodHwa Young Kim, Jung Min Ko
Pediatric Neurology|September 15, 2010
Clinical features and outcomes of holoprosencephaly in KoreaJung Min Ko, Sung Hwan Kim
BMC Medical Genetics|November 29, 2019
A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-upJaehui Ryu, Jung Min Ko, Choong-Ho Shin
Ophthalmic Genetics|February 8, 2014
Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11Jae-hyung Kim, Jung Min Ko, Hungwon Tchah
Pageof 17

Showing results (1-10 of 166) with videos related to

Sort By:
Pageof 17
Journal of Korean Neurosurgical Society|May 27, 2016
Genetic Syndromes Associated with CraniosynostosisJung Min Ko
Korean Circulation Journal|September 29, 2015
Genetic Syndromes associated with Congenital Heart DiseaseJung Min Ko
Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
Genetic syndromes associated with overgrowth in childhoodJung Min Ko
Korean Circulation Journal|March 21, 2018
Chromosomal Microarray: Application for Congenital Heart DiseasesJung Min Ko
Clinical and Experimental Pediatrics|November 21, 2023
Advancing orphan drug development for rare diseasesJung Min Ko
Korean Journal of Pediatrics|October 30, 2015
Kabuki syndrome: clinical and molecular characteristicsChong-Kun Cheon, Jung Min Ko
Annals of Pediatric Endocrinology & Metabolism|July 6, 2022
Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhoodHwa Young Kim, Jung Min Ko
Pediatric Neurology|September 15, 2010
Clinical features and outcomes of holoprosencephaly in KoreaJung Min Ko, Sung Hwan Kim
BMC Medical Genetics|November 29, 2019
A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-upJaehui Ryu, Jung Min Ko, Choong-Ho Shin
Ophthalmic Genetics|February 8, 2014
Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11Jae-hyung Kim, Jung Min Ko, Hungwon Tchah
Pageof 17