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Photodermatology, Photoimmunology & Photomedicine
|
May 8, 2020
Lentigo maligna in a patient with xeroderma pigmentosum, variant type: A case report with dermoscopic findings and review of the literature
Eunsik Bang, Ye Eun Kim, Jung Min Ko, et al.
Brain Communications
|
September 21, 2023
Expansion of clinico-genetic spectrum of <i>PRDX3</i> disease: a literature review with two additional cases
Jaeso Cho, Jihoon G Yoon, Seungbok Lee, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
November 30, 2021
Transcatheter Dynamic Contrast-Enhanced MR Lymphangiography for Nontraumatic Lymphatic Disorders: Technical Feasibility and Imaging Findings
Seunghyun Lee, Saebeom Hur, Dong In Suh, et al.
Annals of Laboratory Medicine
|
October 25, 2022
The First Korean Case of VEXAS Syndrome Caused by a <i>UBA1</i> Somatic Variant
Jihoon G Yoon, Seungbok Lee, Sheehyun Kim, et al.
European Journal of Medical Genetics
|
April 4, 2020
Molecular diagnosis of glycogen storage disease type IX using a glycogen storage disease gene panel
Tae Hyeong Kim, Kwang Yeon Kim, Man Jin Kim, et al.
European Journal of Medical Genetics
|
April 8, 2022
Clinical and molecular delineation of mandibulofacial dysostosis with microcephaly in six Korean patients: When to consider EFTUD2 analysis?
Jae Hui Ryu, Hwa Young Kim, Jung Min Ko, et al.
Annals of Pediatric Endocrinology & Metabolism
|
January 3, 2019
Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy
You Jung Heo, Jung Min Ko, Young Ah Lee, et al.
Journal of Movement Disorders
|
July 8, 2024
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients
Yongmoo Kim, Seungbok Lee, Jae So Cho, et al.
Annals of Laboratory Medicine
|
August 10, 2021
Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome
Boram Kim, Yongsook Park, Sung Im Cho, et al.
European Journal of Human Genetics : EJHG
|
February 2, 2024
Diagnostic uplift through the implementation of short tandem repeat analysis using exome sequencing
Jihoon G Yoon, Seungbok Lee, Jaeso Cho, et al.
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Search research articles
Search
Showing results (21-30 of 95) with videos related to
Sort By:
Page
of 10
Photodermatology, Photoimmunology & Photomedicine
|
May 8, 2020
Lentigo maligna in a patient with xeroderma pigmentosum, variant type: A case report with dermoscopic findings and review of the literature
Eunsik Bang, Ye Eun Kim, Jung Min Ko, et al.
Brain Communications
|
September 21, 2023
Expansion of clinico-genetic spectrum of <i>PRDX3</i> disease: a literature review with two additional cases
Jaeso Cho, Jihoon G Yoon, Seungbok Lee, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
November 30, 2021
Transcatheter Dynamic Contrast-Enhanced MR Lymphangiography for Nontraumatic Lymphatic Disorders: Technical Feasibility and Imaging Findings
Seunghyun Lee, Saebeom Hur, Dong In Suh, et al.
Annals of Laboratory Medicine
|
October 25, 2022
The First Korean Case of VEXAS Syndrome Caused by a <i>UBA1</i> Somatic Variant
Jihoon G Yoon, Seungbok Lee, Sheehyun Kim, et al.
European Journal of Medical Genetics
|
April 4, 2020
Molecular diagnosis of glycogen storage disease type IX using a glycogen storage disease gene panel
Tae Hyeong Kim, Kwang Yeon Kim, Man Jin Kim, et al.
European Journal of Medical Genetics
|
April 8, 2022
Clinical and molecular delineation of mandibulofacial dysostosis with microcephaly in six Korean patients: When to consider EFTUD2 analysis?
Jae Hui Ryu, Hwa Young Kim, Jung Min Ko, et al.
Annals of Pediatric Endocrinology & Metabolism
|
January 3, 2019
Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy
You Jung Heo, Jung Min Ko, Young Ah Lee, et al.
Journal of Movement Disorders
|
July 8, 2024
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients
Yongmoo Kim, Seungbok Lee, Jae So Cho, et al.
Annals of Laboratory Medicine
|
August 10, 2021
Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome
Boram Kim, Yongsook Park, Sung Im Cho, et al.
European Journal of Human Genetics : EJHG
|
February 2, 2024
Diagnostic uplift through the implementation of short tandem repeat analysis using exome sequencing
Jihoon G Yoon, Seungbok Lee, Jaeso Cho, et al.
Page
of 10