Results 1 to 4 of 4
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RET mutational spectrum in Hirschsprung disease: Evaluation of 601 Chinese patientsSo, MT; LeonThomas, YY; Cheng, G; TangClara, SM; Miao, XP; Cornes, BK; Ngo, DN; Cui, L; NganElly, SW; LuiVincent, CH; Wu, XZ; Wang, B; Wang, H; Yuan, ZW; Huang, LM; Li, L; Xia, H; Zhu, D; Liu, J; Nguyen, TL; ChanIvy, HY; ChungPatrick, HY; Liu, XL; Zhang, R; WongKenneth, KY; Sham, PC; Cherny, SS; TamPaul, KH; GarciaBarcelo, MM2011228
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, MM2010701
A RET founder mutation in Chinese hirschsprung's patientsCornes, BK; Tang, CSM; Leon, TYY; So, MT; Sham, PC; Tam, PKH; Garcia-Barcelo, MM200991
Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twinsHur, YM; Kaprio, J; Iacono, WG; Boomsma, DI; McGue, M; Silventoinen, K; Martin, NG; Luciano, M; Visscher, PM; Rose, RJ; He, M; Ando, J; Ooki, S; Nonaka, K; Lin, CCH; Lajunen, HR; Cornes, BK; Bartels, M; Van Beijsterveldt, CEM; Cherny, SS; Mitchell, K2008210
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