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Showing results 1 to 9 of 9

	Title	Author(s)	Issue Date
	CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis Journal:Molecular Genetics & Genomic Medicine	LEUNG, KC Ying, D MAK, CCY Chen, XY Xu, W YEUNG, KS Wong, WL Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Sham, PC Lau, YL Chung, BHY Lee, SL	2017
	The clinical impact of chromosomal microarray on paediatric care in Hong Kong Journal:PLoS ONE	Tao, QV Chan, YK Chu, WY Mok, TKG Tan, TY Yang, W Lee, SL Tang, WF Tso, WYW Lau, ETK Kan, SYA Tang, MHY Lau, YL Chung, BHY	20-Oct-2014
	Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese Journal:npj Genomic Medicine	Chau, FTJ YU, HC Chui, MCM Yeung, CCW Kwok, AWC ZHUANG, X Lee, R Fung, LF LEE, M Mak, CCY Ng, YTN Chung, CY Chung, CY TSANG, HY Chan, JCK Chan, YK Kan, ASY Chung, HY Yang, W Lee, SL Chan, GCF Tam, PKH Lau, YL Yeung, KS Chung, BHY Tang, SM	2022
	Exome sequencing identifies molecular diagnosis in children with drug-resistant epilepsy Journal:Epilepsia Open	Tsang, HY Leung, KC Ho, CCA Yeung, KS Mak, CCY Pei, LCS Yu, HC Kan, SYA Chan, YK Kwong, KL Lee, SL Yung, AWY Fung, CW Chung, BHY	2019
	Expanded Prader-Willi Syndrome Due to Chromosome 15q11.2-14 Deletion: Report and a Review of Literature Journal:American Journal of Medical Genetics, Part A	Liu, APY Tang, WF Lau, ETK Chan, YK Kan, SYA Wong, KY Tso, WYW Jalal, K Lee, SL Chau, CSK Chung, BHY	2013
	Management and outcome of antenatally diagnosed congenital cystic adenomatoid malformation of the lung Journal:Hong Kong Medical Journal	Chow, PC Lee, SL Tang, MHY Chan, KL Lee, CP Lam, BCC Tsoi, NS	2007
	Natural history of infants with vitamin D deficiency in Hong Kong Journal:Asia Pacific Journal of Clinical Nutrition	Tung, JY So, HK Tung, KT Wong, RS Tsang, HW Chan, B Tso, WW Wong, IC Yam, JC Lee, SL Pang, G Wong, WH Cheung, KW Leung, WC Ip, P	30-Dec-2023
	Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay Journal:Journal of Medical Genetics	Yeung, KS Ho, SP Lee, SL Kan, SYA Chan, YK Tang, MHY MAK, CCY Leung, KC So, PL Pfundt, R Marshall, CR Scherer, SW Choufani, S Weksberg, R Chung, BHY	2018
	Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Journal:Molecular Autism	Mak, ASL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, CNV Uddin, M Lee, SL Marshall, CR Scherer, SW Kan, ASY Chung, BHY	2017

Showing results 1 to 9 of 9