Genetic syndromes associated with overgrowth in childhood

por Ko, Jung Min
Publicado 2013

Genetic Syndromes associated with Congenital Heart Disease

por Ko, Jung Min
Publicado 2015

Genetic Syndromes Associated with Craniosynostosis

por Ko, Jung Min
Publicado 2016

Chromosomal Microarray: Application for Congenital Heart Diseases

por Ko, Jung Min
Publicado 2018

Kabuki syndrome: clinical and molecular characteristics

por Cheon, Chong-Kun, Ko, Jung Min
Publicado 2015

Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhood

por Kim, Hwa Young, Ko, Jung Min
Publicado 2022

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-up

por Ryu, Jaehui, Ko, Jung Min, Shin, Choong-Ho
Publicado 2019

Pachyonychia Congenita with a Novel Variant in the KRT16 Gene, c.348_379delinsAA

por Hur, Keunyoung, Ko, Jung Min, Mun, Je-Ho
Publicado 2022

First Korean Family with a Mutation in TPM2 Associated with Sheldon-Hall Syndrome

por Ko, Jung Min, Choi, In-Ho, Baek, Goo-Hyun, Kim, Kee-Won
Publicado 2013

Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases

por Kim, Yoo Jinie, Ko, Jung Min, Song, Junghan, Lee, Kyung-A
Publicado 2018

Flap Extension Technique Using Intrasocket Granulation Tissue in Peri-Implant Osseous Defect: Case Series

por Park, Won-Bae, Ko, Jung-Min, Han, Ji-Young, Kang, Philip
Publicado 2022

Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders

por Kim, Hwa Young, Shin, Choong Ho, Shin, Chang Ho, Ko, Jung Min
Publicado 2023

A Case Report of Rubinstein-Taybi Syndrome Presenting with Extensive Keloid Formation and Review of Literature

por Kim, Jee-Woo, Ko, Jung Min, Lee, Dong Yoon, Shin, Jung-Won
Publicado 2023

Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism

por KO, JUNG MIN, YANG, JUNG-AH, JEONG, SEON-YONG, KIM, HYON-JU
Publicado 2012

A Korean boy with 46,XX testicular disorder of sex development caused by SOX9 duplication

por Lee, Gyung Min, Ko, Jung Min, Shin, Choong Ho, Yang, Sei Won
Publicado 2014

Skewed X-Chromosome Inactivation in a Korean Girl with Severe Mucopolysaccharidosis Type II

por Kim, Hwa Young, Kim, Man Jin, Seong, Moon-Woo, Ko, Jung Min
Publicado 2022

Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome

por Choufani, Sanaa, Ko, Jung Min, Lou, Youliang, Shuman, Cheryl, Fishman, Leona, Weksberg, Rosanna
Publicado 2021

Partial Tetrasomy of Chromosome 22q11.1 Resulting from a Supernumerary Isodicentric Marker Chromosome in a Boy with Cat-eye Syndrome

por Ko, Jung Min, Kim, Jun Bum, Pai, Ki Soo, Yun, Jun-No, Park, Sang-Jin
Publicado 2010

A Korean child diagnosed with malonic aciduria harboring a novel start codon mutation following presentation with dilated cardiomyopathy

por Lee, Seung Hoon, Ko, Jung Min, Song, Mi‐Kyoung, Song, Junghan, Park, Kyung Sun
Publicado 2020

Predictors of cervical myelopathy and hydrocephalus in young children with achondroplasia

por Shim, Youngbo, Ko, Jung Min, Cho, Tae-Joon, Kim, Seung‐Ki, Phi, Ji Hoon
Publicado 2021