E-LIB Suche - Ergebnisse für: Lee, Cha Gon

1

KCNJ3 is a novel candidate gene for autosomal dominant pure..:

Lee, Woong‐Woo ; Lee, Cha Gon ; Ki, Chang‐Seok
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. , 2024

Link: https://doi.org/10.1002/..

2

Effects of once-weekly dulaglutide on juvenile type 2 diabe..:

Seo, Ji Young ; Lee, Cha Gon ; Choi, Hoonsung...
Annals of Pediatric Endocrinology & Metabolism. 28 (2023) 4 - p. 296-301 , 2023

Link: https://doi.org/10.6065/..

3

A Case of Fulminant Type 1 Diabetes Mellitus after Recovery..:

Suh, Dong Woo ; Lee, Cha Gon ; Lee, Hong Kyu.
The Journal of Korean Diabetes. 23 (2022) 4 - p. 278-281 , 2022

Link: https://doi.org/10.4093/..

4

A Novel De Novo Heterozygous ARID1A Missense Variant Cluste..:

Lee, Cha Gon ; Ki, Chang-Seok
Annals of Laboratory Medicine. 41 (2021) 3 - p. 350-353 , 2021

Link: https://doi.org/10.3343/..

5

Dopa-responsive dystonia with additional unusual clinical f..:

Lee, Woong-Woo ; Choi, Jong-Moon ; Lee, Cha Gon
Journal of Genetic Medicine. 17 (2020) 1 - p. 34-38 , 2020

Link: https://doi.org/10.5734/..

6

The first familial case of inherited intellectual developme..:

Lee, Cha Gon ; Seol, Chang Ahn ; Ki, Chang‐Seok
American Journal of Medical Genetics Part A. 182 (2020) 11 - p. 2788-2792 , 2020

Link: https://doi.org/10.1002/..

7

PDE3A variant associated with hypertension and brachydactyl..:

Lee, Cha Gon ; Kang, Kyusik ; Yoon, Ra Gyoung..
European Journal of Medical Genetics. 63 (2020) 4 - p. 103781 , 2020

Link: https://doi.org/10.1016/..

8

Smith-Kingsmore syndrome: The first report of a Korean pati..:

Lee, Dohwan ; Jang, Ja-Hyun ; Lee, Cha Gon
Journal of Genetic Medicine. 16 (2019) 1 - p. 27-30 , 2019

Link: https://doi.org/10.5734/..

9

First identified Korean family with Tatton-Brown-Rahman Syn..:

Lee, Cha Gon ; Jang, Ja-Hyun ; Seo, Ji-Young
Annals of Pediatric Endocrinology & Metabolism. 24 (2019) 4 - p. 253-256 , 2019

Link: https://doi.org/10.6065/..

10

A family with X-linked Cornelia de Lange syndrome due to a ..:

Hong, Sungwon ; Lee, Cha Gon
Journal of Genetic Medicine. 15 (2018) 1 - p. 24-27 , 2018

Link: https://doi.org/10.5734/..

11

Novel compound heterozygous mutations of ATM in ataxia-tela..:

Jang, Min Jeong ; Lee, Cha Gon ; Kim, Hyun Jung
Journal of Genetic Medicine. 15 (2018) 2 - p. 110-114 , 2018

Link: https://doi.org/10.5734/..

12

Multi-gene panel testing in Korean patients with common gen..:

Lee, Cha Gon ; Lee, Jeehun ; Lee, Munhyang.
PLOS ONE. 13 (2018) 6 - p. e0199321 , 2018

Link: https://doi.org/10.1371/..

13

Correction: Identification of a Novel Mutation in BRD4 that..:

Jin, Hyun-Seok ; Kim, Jeonghyung ; Kwak, Woori...
PLOS ONE. 12 (2017) 3 - p. e0173757 , 2017

Link: https://doi.org/10.1371/..

14

Identification of a Novel Mutation in BRD4 that Causes Auto..:

Jin, Hyun-Seok ; Kim, Jeonhyun ; Kwak, Woori...
PLOS ONE. 12 (2017) 1 - p. e0169226 , 2017

Link: https://doi.org/10.1371/..

15

Xeroderma pigmentosum group A with mutational hot spot (c.3..:

Choi, Jung Yoon ; Yun, Hyung Ho ; Lee, Cha Gon
Journal of Genetic Medicine. 13 (2016) 1 - p. 20-25 , 2016

Link: https://doi.org/10.5734/..