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RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.
So MT, Leon TY, Cheng G, Tang CS, Miao XP, Cornes BK, Diem NN, Cui L, Ngan ES, Lui VC, Wu XZ, Wang B, Wang H, Yuan ZW, Huang LM, Li L, Xia H, Zhu D, Liu J, Nguyen TL, Chan IH, Chung PH, Liu XL, Zhang R, Wong KK, Sham PC, Cherny SS, Tam PK, Garcia-Barcelo MM. So MT, et al. Among authors: yuan zw. PLoS One. 2011;6(12):e28986. doi: 10.1371/journal.pone.0028986. Epub 2011 Dec 9. PLoS One. 2011. PMID: 22174939 Free PMC article.
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
Garcia-Barceló M, So MT, Lau DK, Leon TY, Yuan ZW, Cai WS, Lui VC, Fu M, Herbrick JA, Gutter E, Proud V, Li L, Pierre-Louis J, Aleck K, van Heurn E, Belloni E, Scherer SW, Tam PK. Garcia-Barceló M, et al. Among authors: yuan zw. Clin Chem. 2006 Jan;52(1):46-52. doi: 10.1373/clinchem.2005.056192. Epub 2005 Oct 27. Clin Chem. 2006. PMID: 16254195
126 results