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Title	Author(s)	Issue Date
Fine mapping of Hirschsprung’s disease loci in 9q31 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009	Cherny, SS Tang, CSM Sribudiani, Y Miao, XP So, MT Sham, PC Tam, PKH Garcia-Barcelo, MM Hofstra, R	2009
Fine mapping of the 9q31 Hirschsprung's disease locus Journal:Human Genetics	Tang, 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, MM	2010
Fine mapping of the NRG1 hirschsprung's disease locus Journal:PLoS ONE	Tang, CSM Tang, WK So, MT Miao, XP Leung, BMC Yip, BHK Leon, TYY Ngan, ESW Lui, VCH Chen, Y Chan, IHY Chung, HY Liu, XL Wu, XZ Wong, KKY Sham, PC Cherny, SS Tam, PKH GarciaBarceló, MM	2011
Fine mapping of the NRG1 Hirschsprung's-associated gene Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Garcia-Barcelo, MM Tang, C Tang, WK So, MT Sham, PC Cherny, SS Tam, PH	2010
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresia Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Garcia-Barcelo, MM Cheng, G Tang, CSM Liu, X Zhang, R So, MT Wong, EHM Chung, HY Chan, IHY Liu, J Zhong, W Xia, H Yu, J Wong, KKY Cherny, SS Sham, PC Tam, PKH	2012
Functional analyses of RET mutations in Chinese hirschsprung disease patients Journal:Birth Defects Research Part A: Clinical and Molecular Teratology	Leon, TYY So, MT Lui, VCH Hofstra, RMW Tam, PKH Ngan, ESW Garcia-Barcelo, MM	2012
Gene network analysis of candidate loci for human anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Garcia-Barcelo, MM Wong, HEM Ng, CL Lui, VCH So, MT Cherny, SS Sham, PC Tam, PK	2013
Genetic mapping for RET-dependent modifiers in Hirschsprung disease (HSCR) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006	Fong, PY Garcia-Barcelo, MM Sham, PC Ng, PKM Lau, CF So, MT Mak, WW Tam, PKH	2006
Genetic profile of a multiplex Hirschsprung disease family Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting	Tang, SM Karim, MA Zhuang, X So, MT Sham, PC Garcia-Barcelo, MM Tam, PKH	2019
Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes Journal:BMC Medical Genomics	Wong, KL Campbell, DD Ngo, ND Yeung, F Cheng, G Tang, SM Chung, HY Tran, NS So, MT Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2016
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 Journal:Human Molecular Genetics	GarciaBarceló, 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, HY Wong, KKY Sham, PC Cherny, SS Tam, PKH	2010
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease Journal:Proceedings of the National Academy of Sciences of the United States of America	Garcia-Barcelo, MM Tang, CSM Ngan, ESW Lui, VCH Chen, Y So, MT Leon, TYY Miao, XP Shum, CKY Liu, FQ Yeung, MY Yuan, ZW Guo, WH Liu, L Sun, XB Huang, LM Tou, JF Song, YQ Chan, D Cheung, KMC Wong, KKY Cherny, SS Sham, PC Tam, PKH	2009
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease Proceeding/Conference:Neurogastroenterology and Motility	Tam, PKH Tang, CSM Ngan, ESW Lui, VCH Chen, Y So, MT Leon, TYY Miao, XP Shum, CKY Liu, FQ Yeung, MY Yuan, ZW Guo, WH Liu, L Sun, XB Huang, LM Tou, JF Song, YQ Chan, D Cheung, KMC Wong, KKY Cherny, SS Sham, PC Garcia-Barcelo, MM	2009
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 Journal:PLoS Genetics	Tang, CSM Cheng, G So, MT Yip, BHK Miao, XP Wong, EHM Ngan, ESW Lui, VCH Song, YQ Chan, D Cheung, K Yuan, ZW Lei, L Chung, HY Liu, XL Wong, KKY Marshall, CR Scherer, S Cherny, SS Sham, PC Tam, PKH GarciaBarceló, MM	2012
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 Proceeding/Conference:International Congress of Human Genetics, ICHG 2011	Garcia-Barcelo, M Tang, CSM So, MT Marshall, CR Scherer, S Cherny, S Sham, P Tam, P	2011
Genome-wide copy number variation in anorectal malformations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cherny, SS Wong, EHM Cui, L Ng, CL Tang, CSM So, MT Yip, BHK Cheng, G Lui, VCH Sham, PC Tam, PKH Garcia-Barcelo, MM	2012
Genome-wide copy number variation study in anorectal malformations Journal:Human Molecular Genetics	Wong, EHM Cui, L Ng, CL Tang, CSM Liu, X So, MT Yip, BHK Cheng, G Zhang, R Tang, WK Yang, W Lau, YL Baum, L Kwan, P Sun, LD Zuo, XB Ren, YQ Yin, XY Miao, X Liu, JJ Lui, VCH Ngan, ESW Yuan, ZW Zhang, SW Xia, JL Wang, HL Sun, XB Wang, RY Chang, T Chan, IHY Chung, HY Zhang, XJ Wong, KKY Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2013
A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma Journal:Journal of the National Cancer Institute	Ngan, ESW Lang, BHH Liu, T Shum, CKY So, MT Lau, DKC Leon, TYY Cherny, SS Tsai, SY Lo, CY Khoo, US Tam, PKH GarciaBarceló, MM	2009
Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population Journal:PLoS ONE	Cornes, BK Tang, CS Leon, TYY Hui, KJWS So, MT Miao, X Cherny, SS Sham, PC Tam, PKH GarciaBarcelo, MM	2010
Identification of a HOXD13 mutation in a VACTERL patient Journal:American Journal of Medical Genetics, Part A	GarciaBarceló, MM Wong, KKY Lui, VCH Yuan, ZW So, MT Ngan, ESW Miao, XP Chung, HY Khong, PL Tam, PKH	2008

Showing results 19 to 38 of 69 < previous next >