Chao MC - Search Results

1

Aicardi syndrome in a 47, XXY male neonate with lissencephaly and holoprosencephaly.

Chen TH, Chao MC, Lin LC, Jong YJ, Yang SN, Lai YH, Chen HL. Chen TH, et al. Among authors: chao mc. J Neurol Sci. 2009 Mar 15;278(1-2):138-40. doi: 10.1016/j.jns.2008.12.008. Epub 2009 Jan 19. J Neurol Sci. 2009. PMID: 19155022

2

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

3

Feminizing adrenocortical adenoma presenting as heterosexual precocious puberty: report of one case.

Hsiao HP, Chao MC, Lin CY, Chen HL, Chiou SS, Chen BH. Hsiao HP, et al. Among authors: chao mc. Acta Paediatr Taiwan. 2005 Mar-Apr;46(2):97-100. Acta Paediatr Taiwan. 2005. PMID: 16302588

4

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.

5

Small mutations of the DMD gene in Taiwanese families.

Hwa HL, Chang YY, Huang CH, Chen CH, Kao YS, Jong YJ, Chao MC, Ko TM. Hwa HL, et al. Among authors: chao mc. J Formos Med Assoc. 2008 Jun;107(6):463-9. doi: 10.1016/S0929-6646(08)60154-0. J Formos Med Assoc. 2008. PMID: 18583217 Free article.

6

Follow-up study of behavioral development and parenting stress profiles in children with congenital hypothyroidism.

Chao MC, Yang P, Hsu HY, Jong YJ. Chao MC, et al. Kaohsiung J Med Sci. 2009 Nov;25(11):588-95. doi: 10.1016/S1607-551X(09)70561-3. Kaohsiung J Med Sci. 2009. PMID: 19858037 Free article.

7

A Taiwanese boy with congenital generalized lipodystrophy caused by homozygous Ile262fs mutation in the BSCL2 gene.

Huang HH, Chen TH, Hsiao HP, Huang CT, Wang CC, Shiau YH, Chao MC. Huang HH, et al. Among authors: chao mc. Kaohsiung J Med Sci. 2010 Nov;26(11):615-20. doi: 10.1016/S1607-551X(10)70094-2. Kaohsiung J Med Sci. 2010. PMID: 21126715 Free article.

8

3-O-methyldopa levels in newborns: Result of newborn screening for aromatic l-amino-acid decarboxylase deficiency.

Chien YH, Chen PW, Lee NC, Hsieh WS, Chiu PC, Hwu WL, Tsai FJ, Lin SP, Chu SY, Jong YJ, Chao MC. Chien YH, et al. Among authors: chao mc. Mol Genet Metab. 2016 Aug;118(4):259-63. doi: 10.1016/j.ymgme.2016.05.011. Epub 2016 May 16. Mol Genet Metab. 2016. PMID: 27216367

9

Holoprosencephaly and trisomy 13 in a fetus with maternal early gestational amphetamine abuse--a case report.

Tsai EM, Lee JN, Chao MC, Chai CY. Tsai EM, et al. Among authors: chao mc. Gaoxiong Yi Xue Ke Xue Za Zhi. 1993 Dec;9(12):703-6. Gaoxiong Yi Xue Ke Xue Za Zhi. 1993. PMID: 8207770

10

Kallmann syndrome--a case report.

Li CC, Chao MC, Huang SP, Chou YH, Huang CH, Chen AH, Wu YP. Li CC, et al. Among authors: chao mc. Kaohsiung J Med Sci. 2002 Jul;18(7):355-8. Kaohsiung J Med Sci. 2002. PMID: 12380326

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