Tzeng CC - Search Results

1

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

Tzeng CC, Tsai LP, Hwu WL, Lin SJ, Chao MC, Jong YJ, Chu SY, Chao WC, Lu CL. Tzeng CC, et al. Am J Med Genet A. 2005 Feb 15;133A(1):37-43. doi: 10.1002/ajmg.a.30528. Am J Med Genet A. 2005. PMID: 15637705

2

Feasibility of blood spot PCR in large-scale screening of fragile X syndrome in southern Taiwan.

Chow JC, Chen DJ, Lin CN, Chiu CY, Huang CB, Chiu PC, Lin CH, Lin SJ, Tzeng CC. Chow JC, et al. Among authors: tzeng cc. J Formos Med Assoc. 2003 Jan;102(1):12-6. J Formos Med Assoc. 2003. PMID: 12684606

3

Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in Taiwan.

Tzeng CC, Tzeng PY, Sun HS, Chen RM, Lin SJ. Tzeng CC, et al. Among authors: tzeng py. Diagn Mol Pathol. 2000 Jun;9(2):75-80. doi: 10.1097/00019606-200006000-00002. Diagn Mol Pathol. 2000. PMID: 10850542

4

An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome.

Tzeng CC, Lin SJ, Chen YJ, Kuo PL, Jong YJ, Tsai LP, Chen RM. Tzeng CC, et al. Diagn Mol Pathol. 2001 Mar;10(1):34-40. doi: 10.1097/00019606-200103000-00006. Diagn Mol Pathol. 2001. PMID: 11277393

5

Methyl-CpG-binding PCR of bloodspots for confirmation of fragile X syndrome in males.

Tzeng CC, Liou CP, Li CF, Lai MC, Tsai LP, Cho WC, Chang HT. Tzeng CC, et al. J Biomed Biotechnol. 2009;2009:643692. doi: 10.1155/2009/643692. Epub 2009 Nov 4. J Biomed Biotechnol. 2009. PMID: 19893637 Free PMC article.

6

A step-wise diagnosis of fragile X syndrome in Taiwan.

Huang YT, Chiang SC, Tzeng CC, Liu CH, Chien YH, Hwu WL. Huang YT, et al. Among authors: tzeng cc. Acta Paediatr Taiwan. 2004 Mar-Apr;45(2):69-72. Acta Paediatr Taiwan. 2004. PMID: 15335113

7

Identification of bidirectional gene conversion between SMN1 and SMN2 by simultaneous analysis of SMN dosage and hybrid genes in a Chinese population.

Chen TH, Tzeng CC, Wang CC, Wu SM, Chang JG, Yang SN, Hung CH, Jong YJ. Chen TH, et al. Among authors: tzeng cc. J Neurol Sci. 2011 Sep 15;308(1-2):83-7. doi: 10.1016/j.jns.2011.06.002. Epub 2011 Jun 25. J Neurol Sci. 2011. PMID: 21705024

8

Detection of Y-chromosome sequences in patients with X-chromosome abnormalities.

Kuo PL, Wu RC, Lin SJ, Tzeng CC, Liu HS, Huang KE. Kuo PL, et al. Among authors: tzeng cc. J Formos Med Assoc. 1995 Sep;94(9):529-34. J Formos Med Assoc. 1995. PMID: 8696166

9

Pilot fragile X screening in normal population of Taiwan.

Tzeng CC, Cho WC, Kuo PL, Chen RM. Tzeng CC, et al. Diagn Mol Pathol. 1999 Sep;8(3):152-6. doi: 10.1097/00019606-199909000-00008. Diagn Mol Pathol. 1999. PMID: 10565687

10

Detection of Y-chromosomal DNA with marker chromosomes in Turner's syndrome.

Kuo PL, Wu RC, Tzeng CC, Lin SJ, Liu SS, Huang KE. Kuo PL, et al. Among authors: tzeng cc. J Formos Med Assoc. 1995 Aug;94(8):474-80. J Formos Med Assoc. 1995. PMID: 7549576

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