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Journal of Korean Medical Science
|
March 2, 2018
Effect of the Standardization of Diagnostic Tests on the Prevalence of Diabetes Mellitus and Impaired Fasting Glucose
Bora Lee, Ji Sung Lee, Yong Wha Lee, et al.
Annals of Laboratory Medicine
|
March 6, 2012
Novel mutations in CEBPA in Korean Patients with acute myeloid leukemia with a normal karyotype
Sollip Kim, Dong-Hwan Dennis Kim, Jun-Ho Jang, et al.
Journal of Clinical Laboratory Analysis
|
June 18, 2026
Resolving a Complex Neonatal Phenotype by Rapid Trio Whole-Genome Sequencing: A De Novo 11q14.3-q22.3 Deletion and a Splicing-Altering Synonymous ANK1 Variant
Hyun-Woo Lee, Ja-Hyun Jang, Beom Hee Lee, et al.
Annals of Clinical and Laboratory Science
|
March 7, 2013
Identification of PRODH mutations in Korean neonates with type I hyperprolinemia
Mi-Ae Jang, Byung Cheol Kim, Chang-Seok Ki, et al.
Korean Circulation Journal
|
January 21, 2026
Genotype-Driven Prognostication in Dilated Cardiomyopathy
David Hong, Young-Gon Kim, Seung Hyeok Bang, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
March 28, 2015
The t(11;14)(q13;q32) translocation as a poor prognostic parameter for autologous stem cell transplantation in myeloma patients with extramedullary plasmacytoma
Ho-Jin Shin, Kihyun Kim, Je-Jung Lee, et al.
Research Square
|
July 16, 2024
Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome
Sung Eun Wang, Yubao Cheng, Jaechul Lim, et al.
Journal of Korean Medical Science
|
January 18, 2022
Clinical Manifestations and Genetic Analysis of 5 Korean Choroideremia Patients Initially Diagnosed With Retinitis Pigmentosa
Jin Ha Kim, Jung Woo Han, Eun Woo Choi, et al.
Breast Cancer (Tokyo, Japan)
|
September 16, 2025
Prevalence of germline CHEK2 variants in East Asians and Koreans based on population genomic databases
Jong Eun Park, Taeheon Lee, Eun Hye Cho, et al.
Frontiers in Genetics
|
July 3, 2025
Novel causative <i>RYR2</i> indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia
Ju Hyeon Shin, Taek Kyu Park, Sung-A Chang, et al.
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of 9
Search research articles
Search
Showing results (71-80 of 87) with videos related to
Sort By:
Page
of 9
Journal of Korean Medical Science
|
March 2, 2018
Effect of the Standardization of Diagnostic Tests on the Prevalence of Diabetes Mellitus and Impaired Fasting Glucose
Bora Lee, Ji Sung Lee, Yong Wha Lee, et al.
Annals of Laboratory Medicine
|
March 6, 2012
Novel mutations in CEBPA in Korean Patients with acute myeloid leukemia with a normal karyotype
Sollip Kim, Dong-Hwan Dennis Kim, Jun-Ho Jang, et al.
Journal of Clinical Laboratory Analysis
|
June 18, 2026
Resolving a Complex Neonatal Phenotype by Rapid Trio Whole-Genome Sequencing: A De Novo 11q14.3-q22.3 Deletion and a Splicing-Altering Synonymous ANK1 Variant
Hyun-Woo Lee, Ja-Hyun Jang, Beom Hee Lee, et al.
Annals of Clinical and Laboratory Science
|
March 7, 2013
Identification of PRODH mutations in Korean neonates with type I hyperprolinemia
Mi-Ae Jang, Byung Cheol Kim, Chang-Seok Ki, et al.
Korean Circulation Journal
|
January 21, 2026
Genotype-Driven Prognostication in Dilated Cardiomyopathy
David Hong, Young-Gon Kim, Seung Hyeok Bang, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
March 28, 2015
The t(11;14)(q13;q32) translocation as a poor prognostic parameter for autologous stem cell transplantation in myeloma patients with extramedullary plasmacytoma
Ho-Jin Shin, Kihyun Kim, Je-Jung Lee, et al.
Research Square
|
July 16, 2024
Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome
Sung Eun Wang, Yubao Cheng, Jaechul Lim, et al.
Journal of Korean Medical Science
|
January 18, 2022
Clinical Manifestations and Genetic Analysis of 5 Korean Choroideremia Patients Initially Diagnosed With Retinitis Pigmentosa
Jin Ha Kim, Jung Woo Han, Eun Woo Choi, et al.
Breast Cancer (Tokyo, Japan)
|
September 16, 2025
Prevalence of germline CHEK2 variants in East Asians and Koreans based on population genomic databases
Jong Eun Park, Taeheon Lee, Eun Hye Cho, et al.
Frontiers in Genetics
|
July 3, 2025
Novel causative <i>RYR2</i> indel variant with exon and intron involvement inducing exon 13 skipping in a family exhibiting catecholaminergic polymorphic ventricular tachycardia
Ju Hyeon Shin, Taek Kyu Park, Sung-A Chang, et al.
Page
of 9