Results 1 to 5 of 5
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TypeTitleAuthor(s)YearViews
Mutations in the NRG1 gene are associated with Hirschsprung diseaseTang, CSM; Ngan, ESW; Tang, WK; So, MT; Cheng, G; Miao, XP; Leon, TYY; Leung, BMC; Hui, KJWS; Lui, VHC; Chen, Y; Chan, IHY; Chung, PHY; Liu, XL; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH; GarciaBarcelo, MM2012244
 
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 (vol 19, pg 2917, 2010)Garcia-Barcelo, MM; Yeung, MY; Miao, XP; Tang, CSM; Cheng, G; So, MT; Ngan, EW; Lui, VCH; Chen, Y; Liu, XL; Hui, KJWS; Li, L; Guo, WH; Sun, XB; Tou, JF; Chan, KW; Wu, XZ; Song, YQ; Chan, D; Cheung, K; Chung, PHY; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH2011157
 
Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese populationCornes, BK; Tang, CS; Leon, TYY; Hui, KJWS; So, MT; Miao, X; Cherny, SS; Sham, PC; Tam, PKH; GarciaBarcelo, MM2010700
 
Fine mapping of the 9q31 Hirschsprung's disease locusTang, CS; Sribudiani, Y; Miao, XP; De Vries, AR; Burzynski, G; So, MT; Leon, YY; Yip, BH; Osinga, J; Hui, KJWS; Verheij, JBGM; Cherny, SS; Tam, PKH; Sham, PC; Hofstra, RMW; GarciaBarceló, MM2010151
 
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2GarciaBarceló, MM; Yeung, MY; Miao, XP; Tang, CSM; Cheng, G; So, MT; Ngan, ES; Lui, VCH; Chen, Y; Liu, XL; Hui, KJWS; Li, L; Guo, WH; Sun, XB; Tou, JF; Chan, KW; Wu, XZ; Song, YQ; Chan, D; Cheung, K; Chung, PHY; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH2010751
 
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