Jeong SY - Search Results

1

Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.

Sohn YB, Lee CG, Ko JM, Yang JA, Yun JN, Jung EJ, Jin HS, Park SJ, Jeong SY. Sohn YB, et al. Among authors: jeong sy. J Hum Genet. 2013 Feb;58(2):73-7. doi: 10.1038/jhg.2012.135. Epub 2012 Nov 29. J Hum Genet. 2013. PMID: 23190751

2

The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.

Jeong SY, Park SJ, Kim HJ. Jeong SY, et al. J Korean Med Sci. 2006 Feb;21(1):107-12. doi: 10.3346/jkms.2006.21.1.107. J Korean Med Sci. 2006. PMID: 16479075 Free PMC article.

3

Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.

Park SJ, Jeong SY, Kim HJ. Park SJ, et al. Among authors: jeong sy. Cancer Genet Cytogenet. 2006 Apr 1;166(1):56-64. doi: 10.1016/j.cancergencyto.2005.08.022. Cancer Genet Cytogenet. 2006. PMID: 16616112

4

Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1.

Jeong SY, Park SJ, Lee SJ, Park HJ, Kim HJ. Jeong SY, et al. J Korean Med Sci. 2010 May;25(5):804-8. doi: 10.3346/jkms.2010.25.5.804. Epub 2010 Apr 16. J Korean Med Sci. 2010. PMID: 20436723 Free PMC article.

5

A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.

Jeong SY, Kim BY, Kim HJ, Yang JA, Kim OH. Jeong SY, et al. J Hum Genet. 2010 Nov;55(11):764-6. doi: 10.1038/jhg.2010.102. Epub 2010 Aug 19. J Hum Genet. 2010. PMID: 20720557

6

Clinical and genetic characteristics of Korean patients with Gaucher disease.

Jeong SY, Park SJ, Kim HJ. Jeong SY, et al. Blood Cells Mol Dis. 2011 Jan 15;46(1):11-4. doi: 10.1016/j.bcmd.2010.07.010. Epub 2010 Aug 21. Blood Cells Mol Dis. 2011. PMID: 20729108

7

Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.

Jeong SY, Kim SJ, Yang JA, Hong JH, Lee SJ, Kim HJ. Jeong SY, et al. J Hum Genet. 2011 Jun;56(6):469-71. doi: 10.1038/jhg.2011.37. Epub 2011 Apr 14. J Hum Genet. 2011. PMID: 21490608

8

Replicated association between genetic variation in the PARK2 gene and blood pressure.

Jin HS, Hong KW, Kim BY, Kim J, Yoo YH, Oh B, Jeong SY. Jin HS, et al. Among authors: jeong sy. Clin Chim Acta. 2011 Aug 17;412(17-18):1673-7. doi: 10.1016/j.cca.2011.05.026. Epub 2011 May 25. Clin Chim Acta. 2011. PMID: 21635879

9

Age-dependent association of the polymorphisms in the mitochondria-shaping gene, OPA1, with blood pressure and hypertension in Korean population.

Jin HS, Sober S, Hong KW, Org E, Kim BY, Laan M, Oh B, Jeong SY. Jin HS, et al. Among authors: jeong sy. Am J Hypertens. 2011 Oct;24(10):1127-35. doi: 10.1038/ajh.2011.131. Epub 2011 Jul 28. Am J Hypertens. 2011. PMID: 21796221

10

Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism.

Ko JM, Yang JA, Jeong SY, Kim HJ. Ko JM, et al. Among authors: jeong sy. Mol Med Rep. 2012 Apr;5(4):943-8. doi: 10.3892/mmr.2012.764. Epub 2012 Jan 25. Mol Med Rep. 2012. PMID: 22294196 Free PMC article.

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