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MNX1 (HLXB9) mutations in Currarino patients.
Garcia-Barceló MM, Lui VC, So MT, Miao X, Leon TY, Yuan ZW, Ngan ES, Ehsan T, Chung PH, Khong PL, Wong KK, Tam PK. Garcia-Barceló MM, et al. Among authors: so mt. J Pediatr Surg. 2009 Oct;44(10):1892-8. doi: 10.1016/j.jpedsurg.2009.03.039. J Pediatr Surg. 2009. PMID: 19853743
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: so mt. Clin Chem. 2006 Jan;52(1):46-52. doi: 10.1373/clinchem.2005.056192. Epub 2005 Oct 27. Clin Chem. 2006. PMID: 16254195
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. PLoS One. 2011;6(12):e28986. doi: 10.1371/journal.pone.0028986. Epub 2011 Dec 9. PLoS One. 2011. PMID: 22174939 Free PMC article.
No NRG1 V266L in Chinese patients with schizophrenia.
Garcia-Barceló MM, Miao X, Tang CS, So HC, Tang W, Leon TY, So M, Yip B, Chen RY, Cheung EF, Chen EY, Li T, Tam P, Cherny SS, Sham PC. Garcia-Barceló MM, et al. Psychiatr Genet. 2011 Feb;21(1):47-9. doi: 10.1097/YPG.0b013e328341355b. Psychiatr Genet. 2011. PMID: 20978455
Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus.
Garcia-Barceló MM, Lau DK, Ngan ES, Leon TY, Liu T, So M, Miao X, Lui VC, Wong KK, Ganster RW, Cass DT, Croaker GD, Tam PK. Garcia-Barceló MM, et al. Ann Hum Genet. 2008 Mar;72(Pt 2):170-7. doi: 10.1111/j.1469-1809.2007.00403.x. Epub 2007 Dec 12. Ann Hum Genet. 2008. Retraction in: Ann Hum Genet. 2009 Jan;73(1):131. doi: 10.1111/j.1469-1809.2008.00491.x. PMID: 18081917 Retracted.
Fine mapping of the 9q31 Hirschsprung's disease locus.
Tang CS, Sribudiani Y, Miao XP, de Vries AR, Burzynski G, So MT, Leon YY, Yip BH, Osinga J, Hui KJ, Verheij JB, Cherny SS, Tam PK, Sham PC, Hofstra RM, Garcia-Barceló MM. Tang CS, et al. Among authors: so mt. Hum Genet. 2010 Jun;127(6):675-83. doi: 10.1007/s00439-010-0813-8. Epub 2010 Apr 2. Hum Genet. 2010. PMID: 20361209 Free PMC article.
54 results