Education / Career
Article | Molecular genetic characteristics of X-linked retinoschisis in Koreans | ||
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Announcements | Mol Vis 2009; 15:833-843 | Date of publication | 2009년 |
Co-researcher | Kim SY, Ko HS, Yu YS, Hwang JM, Lee JJ, Kim SY, Kim JY, Seong MW, Park KH, Park SS. |
Article | Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation. | ||
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Announcements | Clin Genet 2009: 76: 152–160 | Date of publication | 2009년 |
Co-researcher | Seong MW, Cho S, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim S, Kim J, Park S |
Article | Molecular characterization of Leber congenital amaurosis in Koreans. | ||
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Announcements | Mol Vis 2008;14:1429-36 | Date of publication | 2008년 |
Co-researcher | Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS |
Article | Mitochondrial DNA content is decreased in autosomal dominant optic atrophy. | ||
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Announcements | Neurology 2005; 64(6):966-72 | Date of publication | 2005년 |
Co-researcher | Kim JY, Hwang JM, Ko HS, Seong MW, Park BJ, Park SS |
Article | Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs. | ||
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Announcements | Genome Res. 2002 May;12(5):729-38. | Date of publication | 2002년 |
Co-researcher | Park SS, Stankiewicz P, Bi W, Shaw C, Lehoczky J, Dewar K, Birren B, Lupski JR |
Article | Mitochondrial DNA C4171A/ND1 is a Novel Primary Causative Mutation of Leber's Hereditary Optic Neuropathy with a Good Prognosis. | ||
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Announcements | Annals of Neurology 2002 May;51(5):630-634 | Date of publication | 2002년 |
Co-researcher | Kim JY, Hwang JM, Park SS. |
Article | LCA5, a rare genetic cause of leber congenital amaurosis in Koreans. | ||
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Announcements | Ophthalmic Genet | Date of publication | 2009 |
Co-researcher | Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS. |
Article | Ophthalmoplegia diagnosis. | ||
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Announcements | Ophthalmology | Date of publication | 2009 |
Co-researcher | Hwang JM, Choung HK, Ko HS, Seong MW, Kim JY, Park SS. |
Article | False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophy. | ||
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Announcements | Genet Test Mol Biomarkers. | Date of publication | 2009 |
Co-researcher | Kang SH, Cho SI, Chae JH, Chung KN, Ra EK, Kim SY, Seong MW, Kim JY, Park SS. |
Article | Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population. | ||
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Announcements | Fam Cancer | Date of publication | 2009 |
Co-researcher | Seong MW, Cho SI, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS. |