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Acta Ophthalmologica
|
November 16, 2020
Strabismus in chronic progressive external ophthalmoplegia
Ji Yeon Kim, Hee Kyung Yang, Namju Kim, et al.
Experimental Dermatology
|
March 3, 2021
Importance of extracutaneous organ involvement in determining the clinical severity and prognosis of incontinentia pigmenti caused by mutations in the IKBKG gene
Hwa Young Kim, Hyun Beom Song, Kyu Han Kim, et al.
Brain & Development
|
July 28, 2020
Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy: A newly identified neurometabolic syndrome
Ji Soo Park, Man Jin Kim, Soo Yeon Kim, et al.
The Journal of Molecular Diagnostics : JMD
|
November 27, 2020
SnackVar: An Open-Source Software for Sanger Sequencing Analysis Optimized for Clinical Use
Young-Gon Kim, Man Jin Kim, Jee-Soo Lee, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2020
Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases
Jee-Soo Lee, Kyung Bok Lee, Han Song, et al.
ACS Nano
|
May 3, 2016
Optical Detection of Enzymatic Activity and Inhibitors on Non-Covalently Functionalized Fluorescent Graphene Oxide
Tae Woog Kang, Su-Ji Jeon, Hye-In Kim, et al.
Journal of Medical Genetics
|
November 21, 2020
Characteristics of germline mutations in Korean patients with pheochromocytoma/paraganglioma
Jung Hee Kim, Man Jin Kim, Sung Hye Kong, et al.
Journal of Human Genetics
|
February 7, 2023
Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia
Man Jin Kim, Sheehyun Kim, Seung Won Chae, et al.
Ophthalmic Genetics
|
June 30, 2020
No association between <i>POU4F1, POU4F2, ISL1</i> polymorphisms and normal-tension glaucoma
Jee-Soo Lee, Jin Wook Jeoung, Sohee Oh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Consistent count region-copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data
Man Jin Kim, Sungyoung Lee, Hongseok Yun, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
Acta Ophthalmologica
|
November 16, 2020
Strabismus in chronic progressive external ophthalmoplegia
Ji Yeon Kim, Hee Kyung Yang, Namju Kim, et al.
Experimental Dermatology
|
March 3, 2021
Importance of extracutaneous organ involvement in determining the clinical severity and prognosis of incontinentia pigmenti caused by mutations in the IKBKG gene
Hwa Young Kim, Hyun Beom Song, Kyu Han Kim, et al.
Brain & Development
|
July 28, 2020
Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy: A newly identified neurometabolic syndrome
Ji Soo Park, Man Jin Kim, Soo Yeon Kim, et al.
The Journal of Molecular Diagnostics : JMD
|
November 27, 2020
SnackVar: An Open-Source Software for Sanger Sequencing Analysis Optimized for Clinical Use
Young-Gon Kim, Man Jin Kim, Jee-Soo Lee, et al.
European Journal of Human Genetics : EJHG
|
November 25, 2020
Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases
Jee-Soo Lee, Kyung Bok Lee, Han Song, et al.
ACS Nano
|
May 3, 2016
Optical Detection of Enzymatic Activity and Inhibitors on Non-Covalently Functionalized Fluorescent Graphene Oxide
Tae Woog Kang, Su-Ji Jeon, Hye-In Kim, et al.
Journal of Medical Genetics
|
November 21, 2020
Characteristics of germline mutations in Korean patients with pheochromocytoma/paraganglioma
Jung Hee Kim, Man Jin Kim, Sung Hye Kong, et al.
Journal of Human Genetics
|
February 7, 2023
Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia
Man Jin Kim, Sheehyun Kim, Seung Won Chae, et al.
Ophthalmic Genetics
|
June 30, 2020
No association between <i>POU4F1, POU4F2, ISL1</i> polymorphisms and normal-tension glaucoma
Jee-Soo Lee, Jin Wook Jeoung, Sohee Oh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Consistent count region-copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data
Man Jin Kim, Sungyoung Lee, Hongseok Yun, et al.
Page
of 8