Ki CS - Search Results

1

Spectrum of cognitive impairment in Korean ALS patients without known genetic mutations.

Oh SI, Park A, Kim HJ, Oh KW, Choi H, Kwon MJ, Ki CS, Kim HT, Kim SH. Oh SI, et al. Among authors: ki cs. PLoS One. 2014 Feb 3;9(2):e87163. doi: 10.1371/journal.pone.0087163. eCollection 2014. PLoS One. 2014. PMID: 24498297 Free PMC article.

2

MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature.

Kim HJ, Ki CS, Park Q, Koo HH, Yoo KH, Kim EJ, Kim SH. Kim HJ, et al. Among authors: ki cs. Genes Chromosomes Cancer. 2003 Sep;38(1):8-12. doi: 10.1002/gcc.10235. Genes Chromosomes Cancer. 2003. PMID: 12874781 Review.

3

Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population.

Ki CS, Lee KA, Lee SY, Kim HJ, Cho SS, Park JH, Cho S, Sohn KM, Kim JW. Ki CS, et al. Clin Chem. 2003 Dec;49(12):2078-81. doi: 10.1373/clinchem.2003.024174. Clin Chem. 2003. PMID: 14633881 No abstract available.

4

Evaluation of imprecision for analysis of short tandem repeats by use of mixed blood cells in variable concentrations.

Kong SY, Ki CS, Kim HJ, Lee KO, Bae JC, Kim SH, Kim JW. Kong SY, et al. Among authors: ki cs. Clin Chem. 2004 Nov;50(11):2193-5. doi: 10.1373/clinchem.2004.036103. Clin Chem. 2004. PMID: 15502099 No abstract available.

5

Two novel mutations in the C7 gene in a Korean patient with complement C7 deficiency.

Ki CS, Kim JW, Kim HJ, Choi SM, Ha GY, Kang HJ, Kim WD. Ki CS, et al. J Korean Med Sci. 2005 Apr;20(2):220-4. doi: 10.3346/jkms.2005.20.2.220. J Korean Med Sci. 2005. PMID: 15831990 Free PMC article.

6

Mutation analysis of SPG4 and SPG3A genes and its implication in molecular diagnosis of Korean patients with hereditary spastic paraplegia.

Park SY, Ki CS, Kim HJ, Kim JW, Sung DH, Kim BJ, Lee WY. Park SY, et al. Among authors: ki cs. Arch Neurol. 2005 Jul;62(7):1118-21. doi: 10.1001/archneur.62.7.1118. Arch Neurol. 2005. PMID: 16009769

7

Mutation analysis of the GNE gene in Korean patients with distal myopathy with rimmed vacuoles.

Kim BJ, Ki CS, Kim JW, Sung DH, Choi YC, Kim SH. Kim BJ, et al. Among authors: ki cs. J Hum Genet. 2006;51(2):137-140. doi: 10.1007/s10038-005-0338-5. Epub 2005 Dec 22. J Hum Genet. 2006. PMID: 16372135

8

Lack of a genetic association between the CTLA-4 gene and Graves' disease in Koreans.

Cho HJ, Chung JH, Kim IS, Kim HJ, Cho SH, Ki CS, Kim JW. Cho HJ, et al. Among authors: ki cs. Thyroid. 2006 Mar;16(3):237-41. doi: 10.1089/thy.2006.16.237. Thyroid. 2006. PMID: 16571085

9

A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndrome.

Kim HJ, Yoo EH, Ki CS, Yoo GH, Koo HH, Kim JW, Kim SH. Kim HJ, et al. Among authors: ki cs. Int J Hematol. 2006 Jun;83(5):426-8. doi: 10.1532/IJH97.A30513. Int J Hematol. 2006. PMID: 16787874

10

X-linked Opitz G/BBB syndrome: identification of a novel mutation and prenatal diagnosis in a Korean family.

Cho HJ, Shin MY, Ahn KM, Lee SI, Kim HJ, Ki CS, Kim JW. Cho HJ, et al. Among authors: ki cs. J Korean Med Sci. 2006 Oct;21(5):790-3. doi: 10.3346/jkms.2006.21.5.790. J Korean Med Sci. 2006. PMID: 17043407 Free PMC article.

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