Chang JG - Search Results

1

A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).

Wu JY, Yang CF, Lee CC, Chang JG, Tsai FJ. Wu JY, et al. Among authors: chang jg. Hum Mutat. 2000 Apr;15(4):389-90. doi: 10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU31>3.0.CO;2-0. Hum Mutat. 2000. PMID: 10738004 No abstract available.

2

Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndrome.

Tsai FJ, Hwu WL, Lin SP, Chang JG, Wang TR, Tsai CH. Tsai FJ, et al. Among authors: chang jg. Hum Mutat. 1998;Suppl 1:S18-9. doi: 10.1002/humu.1380110106. Hum Mutat. 1998. PMID: 9452027 No abstract available.

3

Mutation analysis of Wilson disease in Taiwan and description of six new mutations.

Tsai CH, Tsai FJ, Wu JY, Chang JG, Lee CC, Lin SP, Yang CF, Jong YJ, Lo MC. Tsai CH, et al. Among authors: chang jg. Hum Mutat. 1998;12(6):370-6. doi: 10.1002/(SICI)1098-1004(1998)12:6<370::AID-HUMU2>3.0.CO;2-S. Hum Mutat. 1998. PMID: 9829905

4

Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.

Tsai CH, Tsai FJ, Wu JY, Lin SP, Chang JG, Yang CF, Lee CC. Tsai CH, et al. Among authors: chang jg. Hum Mutat. 1999 Dec;14(6):542. doi: 10.1002/(SICI)1098-1004(199912)14:6<542::AID-HUMU14>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10571953

5

Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.

Peng CT, Wu JY, Tsai CH, Tsai FJ, Chang JG. Peng CT, et al. Among authors: chang jg. J Hum Genet. 1998;43(4):237-41. doi: 10.1007/s100380050080. J Hum Genet. 1998. PMID: 9852674

6

No association of alpha-2 macroglobulin gene five-nucleotide deletion with AD in Taiwan Chinese.

Hu CJ, Sung SM, Liu HC, Lee KY, Hsu WC, Wong WK, Lee CC, Tsai CH, Chang JG. Hu CJ, et al. Among authors: chang jg. Neurology. 1999 Aug 11;53(3):642-3. doi: 10.1212/wnl.53.3.642. Neurology. 1999. PMID: 10449138

7

Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations.

Chang JG, Yang TY, Liu TC, Lin TP, Hu CJ, Kao MC, Wang NM, Tsai FJ, Peng CT, Tsai CH. Chang JG, et al. Transfusion. 1999 Sep;39(9):1013-7. doi: 10.1046/j.1537-2995.1999.39091013.x. Transfusion. 1999. PMID: 10533829

8

Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan.

Hu CJ, Sung SM, Liu HC, Lee CC, Tsai CH, Chang JG. Hu CJ, et al. Among authors: chang jg. Eur Neurol. 2000;44(2):90-3. doi: 10.1159/000008203. Eur Neurol. 2000. PMID: 10965160

9

Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan.

Hu CJ, Sung SM, Liu HC, Hsu WC, Lee LS, Lee CC, Tsai CH, Chang JG. Hu CJ, et al. Among authors: chang jg. J Neurol Sci. 2000 Dec 1;181(1-2):127-31. doi: 10.1016/s0022-510x(00)00443-3. J Neurol Sci. 2000. PMID: 11099722

10

Mutation analysis of the tumor suppressor gene PPP2R1B in human cervical cancer.

Yeh LS, Hsieh YY, Chang JG, Chang WW, Chang CC, Tsai FJ. Yeh LS, et al. Among authors: chang ww, chang cc, chang jg. Int J Gynecol Cancer. 2007 Jul-Aug;17(4):868-71. doi: 10.1111/j.1525-1438.2007.00880.x. Epub 2007 Mar 2. Int J Gynecol Cancer. 2007. PMID: 17343570

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