Items for Author "Chao MC" 

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Showing 6 items.

Collection	Date	Title	Authors	Bitstream
[生物醫學研究所] 期刊論文	2010-01-01	Comparing the Southern blot method and PCR product analysis for chimeric-RCCX detection in CYP21A2 deficiency.	Lee HH; Lee YJ; Chao MC
[生物醫學研究所] 期刊論文	2008-01-01	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
[生物醫學研究所] 期刊論文	2007-01-01	Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome.	Hung CS; Lin JL; Lee YJ; Lin SP; Chao MC; Lo FS
[生物醫學研究所] 期刊論文	2014-03-01	Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese	Wu YL; Hwang DW; Hsiao HP; Ting WH; Huang CY; Tsai WY; Chen HC; Chao MC; Lo FS; Tsai JD; Yang S; Shih SL; Lin CL; Lee YJ
[生物醫學研究所] 期刊論文	2009-01-01	Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature.	Lo FS; Lin JL; Kuo MT; Chiu PC; Shu SG; Chao MC; Lee YJ; Lin SP
[生物醫學研究所] 期刊論文	2009-01-01	The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase.	Lee YJ; Tsai LP,; Niu DM; Shu SG; Chao MC; Lee HH