Seong MW - Search Results

1

A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing.

Solomon PJ, Margaret P, Rajendran R, Ramalingam R, Menezes GA, Shirley AS, Lee SJ, Seong MW, Park SS, Seol D, Seo SH. Solomon PJ, et al. Among authors: seong mw. Ital J Pediatr. 2015 May 8;41:38. doi: 10.1186/s13052-015-0142-6. Ital J Pediatr. 2015. PMID: 25953249 Free PMC article. Review.

2

Molecular characterization of Leber congenital amaurosis in Koreans.

Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS. Seong MW, et al. Mol Vis. 2008 Aug 4;14:1429-36. Mol Vis. 2008. PMID: 18682808 Free PMC article.

3

Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.

Kim SY, Kim JY, Kim GP, Sung JJ, Lim KS, Lee KW, Chae JH, Hong YH, Seong MW, Park SS. Kim SY, et al. Among authors: seong mw. Korean J Lab Med. 2008 Dec;28(6):483-92. doi: 10.3343/kjlm.2008.28.6.483. Korean J Lab Med. 2008. PMID: 19127114

4

LCA5, a rare genetic cause of leber congenital amaurosis in Koreans.

Seong MW, Kim SY, Yu YS, Hwang JM, Kim JY, Park SS. Seong MW, et al. Ophthalmic Genet. 2009 Mar;30(1):54-5. doi: 10.1080/13816810802592567. Ophthalmic Genet. 2009. PMID: 19172513

5

Molecular genetic characteristics of X-linked retinoschisis in Koreans.

Kim SY, Ko HS, Yu YS, Hwang JM, Lee JJ, Kim SY, Kim JY, Seong MW, Park KH, Park SS. Kim SY, et al. Among authors: seong mw. Mol Vis. 2009;15:833-43. Epub 2009 Apr 23. Mol Vis. 2009. PMID: 19390641 Free PMC article.

6

False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophy.

Kang SH, Cho SI, Chae JH, Chung KN, Ra EK, Kim SY, Seong MW, Kim JY, Park SS. Kang SH, et al. Among authors: seong mw. Genet Test Mol Biomarkers. 2009 Aug;13(4):511-3. doi: 10.1089/gtmb.2008.0158. Genet Test Mol Biomarkers. 2009. PMID: 19663601

7

Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population.

Seong MW, Cho SI, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS. Seong MW, et al. Fam Cancer. 2009;8(4):505-8. doi: 10.1007/s10689-009-9279-z. Epub 2009 Aug 8. Fam Cancer. 2009. PMID: 19669600

8

Screening for MAPT and PGRN mutations in Korean patients with PSP/CBS/FTD.

Kim HJ, Jeon BS, Yun JY, Seong MW, Park SS, Lee JY. Kim HJ, et al. Among authors: seong mw. Parkinsonism Relat Disord. 2010 May;16(4):305-6. doi: 10.1016/j.parkreldis.2010.01.004. Epub 2010 Feb 19. Parkinsonism Relat Disord. 2010. PMID: 20171924 No abstract available.

9

Predicted pathogenic missense mutation of PGRN found in a normal control.

Kim HJ, Seong MW, Yun JY, Park SS, Lee JY, Jeon BS. Kim HJ, et al. Among authors: seong mw. Ann Neurol. 2010 Mar;67(3):415-6. doi: 10.1002/ana.21892. Ann Neurol. 2010. PMID: 20373362 No abstract available.

10

Molecular characterization of the NF2 gene in Korean patients with neurofibromatosis type 2: a report of four novel mutations.

Seong MW, Yeo IK, Cho SI, Park CK, Kim SK, Paek SH, Kim DG, Jung HW, Park H, Kim SY, Kim JY, Park SS. Seong MW, et al. Korean J Lab Med. 2010 Apr;30(2):190-4. doi: 10.3343/kjlm.2010.30.2.190. Korean J Lab Med. 2010. PMID: 20445339

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