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Park, Sung Sup
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Education / Career

Education / Career
Article Molecular genetic characteristics of X-linked retinoschisis in Koreans
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.
Education / Career
Article Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.
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
Education / Career
Article Molecular characterization of Leber congenital amaurosis in Koreans.
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
Education / Career
Article Mitochondrial DNA content is decreased in autosomal dominant optic atrophy.
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
Education / Career
Article Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs.
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
Education / Career
Article Mitochondrial DNA C4171A/ND1 is a Novel Primary Causative Mutation of Leber's Hereditary Optic Neuropathy with a Good Prognosis.
Announcements Annals of Neurology 2002 May;51(5):630-634 Date of publication 2002년
Co-researcher Kim JY, Hwang JM, Park SS.
Education / Career
Article LCA5, a rare genetic cause of leber congenital amaurosis in Koreans.
Announcements Ophthalmic Genet Date of publication 2009
Co-researcher Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS.
Education / Career
Article Ophthalmoplegia diagnosis.
Announcements Ophthalmology Date of publication 2009
Co-researcher Hwang JM, Choung HK, Ko HS, Seong MW, Kim JY, Park SS.
Education / Career
Article False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophy.
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.
Education / Career
Article Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population.
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.

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