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Showing results 20 to 34 of 34 < previous

	Title	Author(s)	Issue Date	Views
	Pre-implantation genetic diagnosis in Hong Kong Journal:Hong Kong Medical Journal	Ng, EHY Lau, EYL Yeung, WSB Lau, ETK Tang, MHY Ho, PC	2003	90
	A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling Journal:European Journal of Medical Genetics	Luk, HM Wong, VCH Lo, IFM Chan, YK Lau, ETK Kan, SYA Tang, MHY Tang, WF She, WMK Chu, WY Sin, WK Chung, BHY	28-Jan-2014	69
	Prenatal Diagnosis of Agenesis of the Corpus Callosum and Cerebellar Vermian Hypoplasia Associated with a Microdeletion on Chromosome 1p32 Journal:Case Reports in Perinatal Medicine	Shek, NWM Tan, TY Ding, SCK Chung, BHY Lau, ETK Tang, MHY	2013	49
	Prenatal diagnostic service - present Proceeding/Conference:30 years of Medical Genetics in Hong Kong	Lau, ETK	2011	17
	Principle and diagnostic pitfall of PCR and FISH Proceeding/Conference:HA Commissioned Training in O&G. February 28, 2011, Hong Kong.	Lau, ETK	2011	18
	Spread of X Inactivation on Chromosome 15 is Associated with a More Severe Phenotype in a Girl with an Unbalanced t(X;15) Translocation Journal:American Journal of Medical Genetics Part A	Yeung, KS Chee, WYY Luk, HM Kan, ASY Tang, MHY Lau, ETK Shuen, AY Lo, IFM Chan, YK Chung, BHY	2014	57
	Target disruption of MVDP, an aldose reductase-like gene, results in embryonic lethality Proceeding/Conference:CSHL 1996 Mouse Molecular Genetics Meeting	Lau, ETK Law, WS Chang, JC Chung, SK Kan, YW Chung, SSM	1996	116
	Two IUGR foetuses with maternal uniparental disomy of chromosome 6 or UPD(6)mat Journal:Journal of Obstetrics and Gynaecology	Leung, WC Lau, WL Lo, TK Lau, TK Lam, YY Kan, SYA Chan, YK Lau, ETK Tang, MHY	2017	167
	Two unusual cases of haemoglobin Bart’s hydrops fetalis due to uniparental disomy or non-paternity. Journal:Fetal Diagnosis and Therapy: clinical advances and basic research	Kou, KOT Lee, H Lau, B Wong, WS Kan, SYA Tang, MHY Lau, ETK Poon, CF Leung, KY	2014	39
	Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics	Liu, APY Chow, PC Lee, PPW Mok, GTK Tang, WF Lau, ETK Lam, STS Chan, YK Kan, SYA Chau, AKT Cheung, YF Lau, YL Chung, BHY	2014	88
	Update on Basic Science or Lab Technique: Array CGH for Prenatal Diagnosis Proceeding/Conference:Conference in Department of Obstetrics and Gynaecology, The University of Hong Kong	Lau, ETK	2012	24
	Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016	Chung, BHY Mak, SL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Chan, YK Kan, SYA Tang, MHY Lau, ETK Fung, CW Lee, SL	2016	37
	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	159
	Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Chu, YWY Leung, KC Mak, ASL Chiu, TA Mak, CCY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, VCN Lee, SL Marshall, C Scherer, S Kan, SYA Chung, BHY	2016	61
	Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong Journal:PLoS ONE	Kan, SYA Lau, ETK Tang, WF Chan, SSY Ding, SCK Chan, YK Lee, CP Hui, PW Chung, BHY Leung, KY Ma, WLT Leung, WC Tang, MHY	2014	82

Showing results 20 to 34 of 34 < previous