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Showing results 6 to 10 of 10 < previous

	Title	Author(s)	Issue Date	Views
	Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism Journal:Molecular Autism	Yeung, KS Tso, WYW Ip, JKJ MAK, CCY Leung, KC TSANG, HY Ying, D Pei, LCS Lee, SL Yang, W Chung, BHY	2017	98
	Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) Journal:BMC Medical Genomics	Leung, KC Mak, CCY Fung, LF Wong, WHS Tsang, HY Yu, HC Pei, LCS Yeung, KS Mok, TKG Lee, CP Hui, PW Tang, MHY Chan, YK Liu, APY Yang, W Sham, PC Kan, SYA Chung, BHY	2018	111
	NLRP3 Inflammasome Contributes to Host Defense Against Talaromyces marneffei Infection Journal:Frontiers in Immunology	Chan, JFW Tan, YP Kui, L Tsang, CC Pei, LCS Lau, YL Woo, PCY Lee, PPW	2021
	Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020	Chung, BHY Ma, ACH Mak, CCY Yeung, KS Ding, J Pei, LCS Ying, D Chow, PC Yu, HC Hasan, KMM Chen, X Cheung, YF	2020	20
	Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion Journal:Clinical Genetics	Chiu, TA Pei, LCS MAK, CCY Leung, KC YU, HC Lee, SL Vreeburg, M Pfundt, R van der Burgt, I Kleefstra, T Frederic, TMT Nambot, S Faivre, L Bruel, AL Rossi, M Isidor, B Kury, S Cogne, B Besnard, T Willems, M Reijnders, MRF Chung, BHY	2018	138

Showing results 6 to 10 of 10 < previous