Chao MC - 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. Among authors: chao wc, chao mc. 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

[Anthropometric study on Down syndrome in Taiwan].

Lin SJ, Hu SC, Sheu SF, Ho JW, Chiou PC, Chao MC, Wang TR, Tseng RW. Lin SJ, et al. Among authors: chao mc. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991 May-Jun;32(3):158-64. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991. PMID: 1837970 Chinese.

3

Prevalence of permanent primary congenital hypothyroidism in Taiwan.

Tsai WY, Lee JS, Chao MC, Chen LY, Lin SJ, Wu KH, Wang TR, Chen JS, Chuang SM. Tsai WY, et al. Among authors: chao mc. J Formos Med Assoc. 1995 May;94(5):271-3. J Formos Med Assoc. 1995. PMID: 7613262

4

Deletion of the C4-CYP21 repeat module leading to the formation of a chimeric CYP21P/CYP21 gene in a 9.3-kb fragment as a cause of steroid 21-hydroxylase deficiency.

Lee HH, Chang SF, Lee YJ, Raskin S, Lin SJ, Chao MC, Lo FS, Lin CY. Lee HH, et al. Among authors: chao mc. Clin Chem. 2003 Feb;49(2):319-22. doi: 10.1373/49.2.319. Clin Chem. 2003. PMID: 12560361 No abstract available.

5

DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.

Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, Gwinn-Hardy K, Yang CC, Wu RM, Chen TF, Wang HC, Chao MC, Chiu MJ, Lu CJ, Lee-Chen GJ. Wang CK, et al. Among authors: chao mc. Eur Neurol. 2004;52(2):96-100. doi: 10.1159/000079938. Epub 2004 Jul 22. Eur Neurol. 2004. PMID: 15273431

6

Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversal.

Hsiao HP, Tsai LP, Chao MC, Tseng HI, Chang YC. Hsiao HP, et al. Among authors: chao mc. J Formos Med Assoc. 2006 Dec;105(12):1013-6. doi: 10.1016/S0929-6646(09)60286-2. J Formos Med Assoc. 2006. PMID: 17185244 Free article.

7

Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Yen JL, Lee YJ, Huang CY, Hung HY, Hsu CH, Kao HA, Chang JH, Chiu NC, Ho CS, Chao MC, Niu DM, Tsai LP, Kuo PL. Lin HY, et al. Among authors: chao mc. Pediatr Int. 2007 Jun;49(3):375-9. doi: 10.1111/j.1442-200X.2007.02368.x. Pediatr Int. 2007. PMID: 17532839

8

Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan.

Lin HY, Lin SP, Chuang CK, Chen MR, Yen JL, Lee YJ, Huang CY, Tsai LP, Niu DM, Chao MC, Kuo PL. Lin HY, et al. Among authors: chao mc. Acta Paediatr. 2007 Jun;96(6):902-5. doi: 10.1111/j.1651-2227.2007.00284.x. Acta Paediatr. 2007. PMID: 17537021

9

Multiplex ligation-dependent probe amplification identification of deletions and duplications of the Duchenne muscular dystrophy gene in Taiwanese subjects.

Hwa HL, Chang YY, Chen CH, Kao YS, Jong YJ, Chao MC, Ko TM. Hwa HL, et al. Among authors: chao mc. J Formos Med Assoc. 2007 May;106(5):339-46. doi: 10.1016/S0929-6646(09)60318-1. J Formos Med Assoc. 2007. PMID: 17561468 Free article.

10

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.

Lee HH, Lee YJ, Wang YM, Chao HT, Niu DM, Chao MC, Tsai FJ, Lo FS, Lin SJ. Lee HH, et al. Among authors: chao ht, chao mc. Mol Genet Metab. 2008 Apr;93(4):450-7. doi: 10.1016/j.ymgme.2007.10.008. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18039588

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