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Showing results 14 to 23 of 23 < previous

	Title	Author(s)	Issue Date
	MNX1 (HLXB9) mutations in Currarino patients Journal:Journal of Pediatric Surgery	GarciaBarceló, MM Lui, VCH So, MT Miao, X Leon, TYY Yuan, ZW Ngan, ESW Ehsan, T Chung, HY Khong, Pl Wong, KKY Tam, PKH	2009
	Mutational analysis of SHH and GLI3 in anorectal malformations Journal:Birth Defects Research Part A - Clinical and Molecular Teratology	GarciaBarceló, MM Lui, VCH Miao, X So, MT Leon, TYY Yuan, ZW Li, L Liu, L Wang, B Sun, XB Huang, LM Tou, JF Ngan, ESW Cherny, SS Chan, KW Lee, KH Wang, W Wong, KKY Tam, PKH	2008
	Mutations in the NRG1 gene are associated with Hirschsprung disease Journal:Human Genetics	Tang, CSM Ngan, ESW Tang, WK So, MT Cheng, G Miao, XP Leon, TYY Leung, BMC Hui, KJWS Lui, VHC Chen, Y Chan, IHY Chung, HY Liu, XL Wong, KKY Sham, PC Cherny, SS Tam, PKH GarciaBarcelo, MM	2012
	De novo mutations associated with sporadic cases of Caudal regresion syndrome Proceeding/Conference:European Journal of Human Genetics	Porsch, RM Merello, E De Marco, P So, MT Sham, PC Tam, PKH Cherny, SS Capra, V Garcia-Barcelo, MM Campbell, DD	2014
	Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis Journal:BMC Medical Genomics	Cheng, G Chung, HY Chan, EKW So, MT Sham, PC Cherny, SS Tam, PKH Garcia-Barcelo, MM	2017
	Perturbation of Hoxb5 Signaling in Vagal Neural Crests Down-Regulates Ret Leading to Intestinal Hypoganglionosis in Mice Journal:Gastroenterology	Lui, VCH Cheng, WWC Leon, TYY Lau, DKC GarciaBareclo, M Miao, XP Kam, MKM So, MT Chen, Y Wall, NA Sham, MH Tam, PKH	2008
	Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome Journal:Clinical Chemistry	GarciaBarceló, M So, MT Lau, DKC Leon, TYY Yuan, ZW Cai, WS Lui, VCH Fu, M Herbrick, JA Gutter, E Proud, V Li, L PierreLouis, J Aleck, K Van Heurn, E Belloni, E Scherer, SW Tam, PKH	2006
	Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease Journal:Human Molecular Genetics	Tang, SM Gui, H Kapoor, A Kim, JH Luzon-Toro, B Pelet, A Burzynski, G Lantieri, F So, MT Berrios, C Shin, HD Fernandez, RM Le, TL Verheij, JBGM Matera, I Cherny, SS Nandakumar, P Cheong, HS Antinolo, G Amiel, J Seo, JM Kim, DY Oh, JT Lyonnet, S Borrego, S Ceccherini, I Hofstra, RMW Chakravarti, A Kim, HY Sham, PC Tam, PKH Garcia-Barcelo, MM	2016
	TTF-1 and RET promoter SNPs: Regulation of RET transcription in Hirschsprung's disease Journal:Human Molecular Genetics	GarciaBarcelo, M Ganster, RW Lui, VCH Leon, TYY So, MT Lau, AMF Fu, M Sham, MH Knight, J Zannini, MS Sham, PC Tam, PKH	2005
	Whole genome sequencing implicates rare variants in sporadic Hirschsprung disease Proceeding/Conference:European Human Genetics Conference (ESHG) 2017	Tang, SM ZHUANG, X So, MT Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2017

Showing results 14 to 23 of 23 < previous