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/vufind/Search/Results?lookfor=%22Lee%2C+Jee-Soo%22&type=Person&sort=year
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PubPharm (87)
1
Comparison of Measurable Residual Disease in Pediatric B-Lymphoblastic Leukemia Using Multiparametric Flow Cytometry and Next-Generation Sequencing
enthalten in:
Annals of laboratory medicine
| 2024
von
Hwang, S.
|
Oh, I.
|
Kwon, S.
| +2
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2
Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation
enthalten in:
International journal of molecular sciences
| 2024
von
Lee, H.
|
Chae, S.
|
Cho, S.
| +3
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3
Analysis of HTT CAG repeat expansion among healthy individuals and patients with chorea in Korea
enthalten in:
Parkinsonism & related disorders
| 2024
von
Kim, R.
|
Seong, M.
|
Oh, B.
| +7
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4
The First Case of Congenital Nephrogenic Diabetes Insipidus Caused by AVPR2 Disruption Because of 4q25 Insertional Translocation
enthalten in:
Annals of laboratory medicine
| 2024
von
Kim, B.
|
Ahn, Y.
|
Park, J.
| +6
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5
Clinical Practice Guideline for Blood-based Circulating Tumor DNA Assays
enthalten in:
Annals of laboratory medicine
| 2024
von
Lee, J.
|
Cho, E.
|
Kim, B.
| +10
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6
Acral Pigmentation in Peutz-Jeghers Syndrome : Dermoscopic Findings and Treatment with the Q-Switched Nd:YAG Laser
enthalten in:
Annals of dermatology
| 2023
von
Shin, H.
|
Hur, K.
|
Lee, J.
| +2
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7
A Case of Genetically Confirmed Pseudohypoparathyroidism Type 1a Presented with Multifocal Plate-Like Osteoma Cutis and Review of Literature
enthalten in:
Annals of dermatology
| 2023
von
Kim, J.
|
Kim, M.
|
Kim, B.
| +3
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8
Variant Allele Frequency of Pseudogene-Related Variants in Short-read Next-Generation Sequencing Data May Mislead Genetic Diagnosis : A Case of Shwachman-Diamond Syndrome
enthalten in:
Annals of laboratory medicine
| 2023
von
Lee, H.
|
Lee, J.
|
Lee, H.
| +4
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9
The Korean Genetic Diagnosis Program for Rare Disease Phase II : outcomes of a 6-year national project
enthalten in:
European journal of human genetics : EJHG
| 2023
von
Kim, M.
|
Kim, B.
|
Lee, H.
| +11
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10
A case of donor cell leukemia driven by a de novo NRAS mutation with complex karyotype
enthalten in:
Annals of hematology
| 2023
von
Jeong, D.
|
Gu, J.
|
Seo, M.
| +5
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87
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Zeitschriftentitel
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Annals of laboratory medicine
9
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4
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3
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3
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Journal of glaucoma
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1
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Thema
56
Journal Article
16
Research Support, Non-U.S. Gov't
9
Case Reports
9
Letter
6
COVID-19
5
Circulating Tumor DNA
5
SARS-CoV-2
4
Biomarkers, Tumor
3
Antigen
3
Biomarkers
3
EC 2.7.11.1
3
Evaluation Study
3
Genotype-phenotype correlation
3
Hypoxia-inducible factor 1
3
RNA, Viral
3
RT-PCR
3
Review
3
Saliva
3
circulating tumor DNA
3
von Hippel-Lindau Tumor suppressor protein
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Erscheinungszeitraum
49
2020-
38
2010-2019
Erscheinungsjahr(e)
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Sprache
80
Englisch
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