In G. Lee

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 14 publications

Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay.

Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay.

Journal: Frontiers in pediatrics

Published: May 07, 2020

Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure.

Seizure duration may increase thyroid-stimulating hormone levels in children experiencing a seizure.

Journal: The Journal of international medical research

Published: November 28, 2019

Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability.

Genetic tests by next-generation sequencing in children with developmental delay and/or intellectual disability.

Journal: Clinical and experimental pediatrics

Published: July 15, 2019

Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability.

Targeted Next-Generation Sequencing of Korean Patients With Developmental Delay and/or Intellectual Disability.

Journal: Frontiers in pediatrics

Published: October 17, 2018

Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience.

Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience.

Journal: Annals of human genetics

Published: July 31, 2018

Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea.

Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea.

Journal: Annals of laboratory medicine

Published: May 27, 2018

Primary headaches in children and adolescents - experiences at a single headache center in Korea.

Primary headaches in children and adolescents - experiences at a single headache center in Korea.

Journal: BMC neurology

Published: December 26, 2017

A Novel Inherited Mutation of SCN8A in a Korean Family with Benign Familial Infantile Epilepsy Using Diagnostic Exome Sequencing.

A Novel Inherited Mutation of SCN8A in a Korean Family with Benign Familial Infantile Epilepsy Using Diagnostic Exome Sequencing.

Journal: Annals of clinical and laboratory science

Published: December 22, 2017

Efficacy of levetiracetam for neonatal seizures in preterm infants.

Efficacy of levetiracetam for neonatal seizures in preterm infants.

Journal: BMC pediatrics

Published: August 25, 2017

Identification of a novel de novo nonsense mutation of the NSD1 gene in monozygotic twins discordant for Sotos syndrome.

Identification of a novel de novo nonsense mutation of the NSD1 gene in monozygotic twins discordant for Sotos syndrome.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 21, 2017

The first patient with sporadic X-linked intellectual disability with de novo ZDHHC9 mutation identified by targeted next-generation sequencing.

The first patient with sporadic X-linked intellectual disability with de novo ZDHHC9 mutation identified by targeted next-generation sequencing.

Journal: European journal of medical genetics

Published: March 17, 2017

Diagnostic exome sequencing identifies a heterozygous MBD5 frameshift mutation in a family with intellectual disability and epilepsy.

Diagnostic exome sequencing identifies a heterozygous MBD5 frameshift mutation in a family with intellectual disability and epilepsy.

Journal: European journal of medical genetics

Published: February 24, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026