HKU Scholars Hub: Browsing DSpace

Browsing "Department of Psychiatry" by Author cheng, g

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date
	Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cheng, G Wong, EHM Sham, PC Cherny, SS Maas, S Scherer, SW Marshall, CR Pereira, SL Tam, PKH Garcia-Barcelo, MM	2012
	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
	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 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
	Integrating genetic analysis with phenotypes of biliary atresia Proceeding/Conference:European Human Genetics Conference, ESHG 2015	Cheng, G Chung, HY Tang, WK Wong, WH Chan, EK So, MT Sham, PC Cherny, SS Tam, PKH Garcia-Barcelo, MM	2015
	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
	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
	RET mutational spectrum in Hirschsprung disease: Evaluation of 601 Chinese patients Journal:PLoS ONE	So, 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 Chung, HY Liu, XL Zhang, R Wong, KKY Sham, PC Cherny, SS Tam, PKH GarciaBarcelo, MM	2011
	Sacral agenesis: a pilot whole exome sequencing and copy number study Journal:BMC Medical Genetics	Porsch, RM Merello, E De Marco, P Cheng, G Rodriguez, L So, MT Sham, PC Tam, PKH Capra, V Cherny, SS Garcia-Barcelo, MM Campbell, DD	2016

Showing results 1 to 11 of 11