Lin WL - Search Results

1

Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR.

Hung CC, Lin SY, Lin SP, Niu DM, Lee NC, Cheng WF, Chen CP, Lin WL, Lee CN, Su YN. Hung CC, et al. Among authors: lin sy, lin wl, lin sp. Electrophoresis. 2009 Jan;30(2):410-6. doi: 10.1002/elps.200800225. Electrophoresis. 2009. PMID: 19137525

2

Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test.

Su YN, Hung CC, Li H, Lee CN, Cheng WF, Tsao PN, Chang MC, Yu CL, Hsieh WS, Lin WL, Hsu SM. Su YN, et al. Among authors: lin wl. Hum Mutat. 2005 May;25(5):460-7. doi: 10.1002/humu.20160. Hum Mutat. 2005. PMID: 15832310

3

Denaturing HPLC coupled with multiplex PCR for rapid detection of large deletions in Duchenne muscular dystrophy carriers.

Hung CC, Su YN, Lin CY, Yang CC, Lee WT, Chien SC, Lin WL, Lee CN. Hung CC, et al. Among authors: lin cy, lin wl. Clin Chem. 2005 Jul;51(7):1252-6. doi: 10.1373/clinchem.2004.046144. Clin Chem. 2005. PMID: 15976104 No abstract available.

4

Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: application to the SMN1/SMN2 gene.

Hung CC, Lee CN, Chen CP, Jong YJ, Chen CA, Cheng WF, Lin WL, Su YN. Hung CC, et al. Among authors: lin wl. Anal Chem. 2005 Nov 1;77(21):6960-8. doi: 10.1021/ac0512047. Anal Chem. 2005. PMID: 16255596

5

A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay.

Lin CY, Su YN, Lee CN, Hung CC, Cheng WF, Lin WL, Chen CA, Hsieh ST. Lin CY, et al. Among authors: lin wl. J Hum Genet. 2006;51(3):227-235. doi: 10.1007/s10038-005-0350-9. Epub 2006 Feb 4. J Hum Genet. 2006. PMID: 16463004

6

Molecular and clinical analyses of 84 patients with tuberous sclerosis complex.

Hung CC, Su YN, Chien SC, Liou HH, Chen CC, Chen PC, Hsieh CJ, Chen CP, Lee WT, Lin WL, Lee CN. Hung CC, et al. Among authors: lin wl. BMC Med Genet. 2006 Sep 18;7:72. doi: 10.1186/1471-2350-7-72. BMC Med Genet. 2006. PMID: 16981987 Free PMC article.

7

Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in Prader-Willi syndrome and Duchenne muscular dystrophy.

Hung CC, Chen CP, Lin SP, Chien SC, Lee CN, Cheng WF, Hsieh WS, Liu MS, Su YN, Lin WL. Hung CC, et al. Among authors: lin wl, lin sp. Clin Chem. 2006 Dec;52(12):2203-10. doi: 10.1373/clinchem.2006.071118. Epub 2006 Oct 13. Clin Chem. 2006. PMID: 17040959

8

Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE.

Hung CC, Su YN, Tsao PN, Chen PC, Lin SJ, Lin CH, Mu SC, Liu CA, Chang YC, Lin WL, Hsieh WS, Hsu SM. Hung CC, et al. Among authors: lin ch, lin wl, lin sj. Electrophoresis. 2007 Mar;28(6):894-9. doi: 10.1002/elps.200600383. Electrophoresis. 2007. PMID: 17300129

9

Molecular assay of -alpha(3.7) and -alpha(4.2) deletions causing alpha-thalassemia by denaturing high-performance liquid chromatography.

Hung CC, Lee CN, Chen CP, Jong YJ, Hsieh WS, Lin WL, Su YN, Hsu SM. Hung CC, et al. Among authors: lin wl. Clin Biochem. 2007 Jul;40(11):817-21. doi: 10.1016/j.clinbiochem.2007.03.018. Epub 2007 Apr 6. Clin Biochem. 2007. PMID: 17512924

10

Use of multiplex PCR and CE for gene dosage quantification and its biomedical applications for SMN, PMP22, and alpha-globin genes.

Hung CC, Chien SC, Lin CY, Chang CH, Chang YF, Jong YJ, Hsieh ST, Hsieh WS, Liu MS, Lin WL, Lee CN, Su YN. Hung CC, et al. Among authors: lin cy, lin wl. Electrophoresis. 2007 Aug;28(16):2826-34. doi: 10.1002/elps.200600647. Electrophoresis. 2007. PMID: 17640091

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