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Year | Number of Results |
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2023 | 3 |
2024 | 2 |
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Page 1
The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project.
Eur J Hum Genet. 2023 Oct;31(10):1147-1153. doi: 10.1038/s41431-023-01415-8. Epub 2023 Jul 6.
Eur J Hum Genet. 2023.
PMID: 37414863
Clinical Trial.
Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia.
Kim MJ, Kim S, Chae SW, Lee S, Yoon JG, Kim B, Lee JS, Chae JH, Seong MW, Moon J.
Kim MJ, et al. Among authors: chae sw.
J Hum Genet. 2023 Jun;68(6):369-374. doi: 10.1038/s10038-023-01122-8. Epub 2023 Feb 7.
J Hum Genet. 2023.
PMID: 36747106
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Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation.
Lee H, Chae SW, Cho SI, Lee JS, Kim MJ, Seong MW.
Lee H, et al. Among authors: chae sw.
Int J Mol Sci. 2024 Feb 28;25(5):2811. doi: 10.3390/ijms25052811.
Int J Mol Sci. 2024.
PMID: 38474058
Free PMC article.
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The First Case of Congenital Nephrogenic Diabetes Insipidus Caused by AVPR2 Disruption Because of 4q25 Insertional Translocation.
Kim B, Ahn YH, Park JH, Lim HS, Chae SW, Lee JS, Kang HG, Kim MJ, Seong MW.
Kim B, et al. Among authors: chae sw.
Ann Lab Med. 2024 May 1;44(3):303-305. doi: 10.3343/alm.2023.0361. Epub 2023 Dec 26.
Ann Lab Med. 2024.
PMID: 38145893
Free PMC article.
No abstract available.
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