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Hemoglobin Yamagata: hemoglobin variant detected by HbA1c test

Annals of laboratory medicine, 2009-12, Vol.29 (6), p.536-540

2009

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Reporting Quality of Diagnostic Accuracy Studies in Laboratory Medicine: Adherence to Standards for Reporting of Diagnostic Accuracy Studies (STARD) 2015

Annals of Laboratory Medicine, 2020, 40(3), , pp.245-252

2020

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The First Korean Case of De Novo Proximal 4p Deletion Syndrome in a Child With Developmental Delay

Annals of Laboratory Medicine, 2020, 40(5), , pp.435-437

2020

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Evaluation of the Triage TOX Drug Screen Assay for Detection of 11 Drugs of Abuse and Therapeutic Drugs

Annals of Laboratory Medicine, 2017, 37(6), , pp.522-525

2017

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Dose Estimation Curves Following In Vitro X-ray Irradiation Using Blood From Four Healthy Korean Individuals

Annals of Laboratory Medicine, 2019, 39(1), , pp.91-95

2019

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Clinical Usefulness of Human Epididymis Protein 4 in Lung Cancer

Annals of Laboratory Medicine, 2017, 37(6), , pp.526-530

2017

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Correspondence: Response to "Evaluating the Cumulative Impact of Ionizing Radiation Exposure With Diagnostic Genetics"

Annals of Laboratory Medicine, 2019, 39(4), , pp.419-420

2019

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A Case of Chronic Myeloid Leukemia With Rare Variant ETV6/ABL1 Rearrangement

Annals of Laboratory Medicine, 2017, 37(1), , pp.77-80

2017

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Effect of Accreditation on the Accuracy of Diagnostic Hematologic Tests: Standard Deviation Index Analysis

Annals of Laboratory Medicine, 2018, 38(1), , pp.67-70

2018

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Effect of Accreditation on Accuracy of Diagnostic Tests in Medical Laboratories

Annals of Laboratory Medicine, 2017, 37(3), , pp.213-222

2017

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A Novel Pathogenic RS1 Variant (c.362delA) in a Korean Patient With Late-onset X-linked Retinoschisis

Annals of Laboratory Medicine, 2019, 39(1), , pp.109-112

2019

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Novel pathogenic variant (c.3178G>A) in the SMC1A gene in a family with Cornelia de Lange syndrome identified by exome sequencing

Annals of Laboratory Medicine, 2015, 35(6), , pp.639-642

2015

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Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea

Annals of Laboratory Medicine, 2015, 35(3), , pp.362-365

2015

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Budget Impact of the Accreditation Program for Clinical Laboratories on Colorectal Cancer Screening via Fecal Immunochemical Testing: Results from the National Cancer Screening Program in Korea

Annals of Laboratory Medicine, 2018, 38(3), , pp.249-254

2018

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Isolation and identification of Geosmithia argillacea from a fungal ball in the lung of a tuberculosis patient

Annals of Laboratory Medicine, 2013, 33(2), , pp.136-140

2013

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Evaluation of the iNtRON VRE vanA/vanB real-time PCR assay for detection of vancomycin-resistant enterococci

Annals of Laboratory Medicine, 2015, 35(1), , pp.76-81

2015

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Simultaneous occurrence of angioimmunoblastic T-cell lymphoma and plasma cell leukemia

Annals of Laboratory Medicine, 2015, 35(1), , pp.149-151

2015

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A novel mutation (c.200T>C) in the NAGLU gene of a Korean patient with mucopolysaccharidosis IIIB

Annals of Laboratory Medicine, 2013, 33(3), , pp.221-224

2013

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The first Korean case of childhood acute myeloid leukemia with inv(11)(p15q22)/NUP98-DDX10 rearrangement: a rare but recurrent genetic abnormality

Annals of Laboratory Medicine, 2014, 34(6), , pp.478-480

2014

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First report on familial hemophagocytic lymphohistiocytosis with an abnormal immunophenotype and T cell monoclonality in Korea

Annals of Laboratory Medicine, 2015, 35(1), , pp.155-158

2015

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Identification of a rare 3 bp BRAF gene deletion in a thyroid nodule by mutant enrichment with 3'-modified oligonucleotides polymerase chain reaction

Annals of Laboratory Medicine, 2012, 32(3), , pp.238-241

2012

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A Novel Mutation (c.200T>C) in the NAGLU Gene of a Korean Patient with copolysaccharidosis IIIB

Annals of laboratory medicine, 2013-05, Vol.33 (3), p.221-224

2013

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Mycobacterial Infection after Intravesical Bacillus Calmette-Gu?rin Treatment for Bladder Cancer: A Case Report

Annals of laboratory medicine, 2011-07, Vol.31 (3), p.197-200

2011

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Hemoglobin Yamagata: hemoglobin variant detected by HbA1c test

Reporting Quality of Diagnostic Accuracy Studies in Laboratory Medicine: Adherence to Standards for Reporting of Diagnostic Accuracy Studies (STARD) 2015

The First Korean Case of De Novo Proximal 4p Deletion Syndrome in a Child With Developmental Delay

Evaluation of the Triage TOX Drug Screen Assay for Detection of 11 Drugs of Abuse and Therapeutic Drugs

Dose Estimation Curves Following In Vitro X-ray Irradiation Using Blood From Four Healthy Korean Individuals

Clinical Usefulness of Human Epididymis Protein 4 in Lung Cancer

Correspondence: Response to "Evaluating the Cumulative Impact of Ionizing Radiation Exposure With Diagnostic Genetics"

A Case of Chronic Myeloid Leukemia With Rare Variant ETV6/ABL1 Rearrangement

Effect of Accreditation on the Accuracy of Diagnostic Hematologic Tests: Standard Deviation Index Analysis

Effect of Accreditation on Accuracy of Diagnostic Tests in Medical Laboratories

A Novel Pathogenic RS1 Variant (c.362delA) in a Korean Patient With Late-onset X-linked Retinoschisis

Novel pathogenic variant (c.3178G>A) in the SMC1A gene in a family with Cornelia de Lange syndrome identified by exome sequencing

Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea

Budget Impact of the Accreditation Program for Clinical Laboratories on Colorectal Cancer Screening via Fecal Immunochemical Testing: Results from the National Cancer Screening Program in Korea

Isolation and identification of Geosmithia argillacea from a fungal ball in the lung of a tuberculosis patient

Evaluation of the iNtRON VRE vanA/vanB real-time PCR assay for detection of vancomycin-resistant enterococci

Simultaneous occurrence of angioimmunoblastic T-cell lymphoma and plasma cell leukemia

A novel mutation (c.200T>C) in the NAGLU gene of a Korean patient with mucopolysaccharidosis IIIB

The first Korean case of childhood acute myeloid leukemia with inv(11)(p15q22)/NUP98-DDX10 rearrangement: a rare but recurrent genetic abnormality

First report on familial hemophagocytic lymphohistiocytosis with an abnormal immunophenotype and T cell monoclonality in Korea

Identification of a rare 3 bp BRAF gene deletion in a thyroid nodule by mutant enrichment with 3'-modified oligonucleotides polymerase chain reaction

A Novel Mutation (c.200T>C) in the NAGLU Gene of a Korean Patient with copolysaccharidosis IIIB

Mycobacterial Infection after Intravesical Bacillus Calmette-Gu?rin Treatment for Bladder Cancer: A Case Report

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