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	Title	Author(s)	Issue Date
	Echogenic and Cystic Fetal Lung Lesions: Evaluation by Prenatal Sonography and Postnatal Imaging Journal:Hong Kong Journal of Radiology	Ho, G Cheung, KW Lam, HL Ip, JKJ Tang, MHY Lam, WWM	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
	Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: What would be missed, who should decide? Journal:Hong Kong Medical Journal	Leung, WC Lau, ET Lau, WL Tang, R Wong, SF Lau, TK Tse, KT Wong, SF To, WK Ng, LKL Lao, TT Tang, MHY	2008
	Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong Journal:Hong Kong Medical Journal	Ng, PPY Tang, MHY Lau, ET Ng, LKL Ng, EHY Tam, PC Yeung, WSB Ho, PC	2009
	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
	Expanded Carrier Screening in Chinese Population – A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women Journal:Frontiers in Genetics	Cheng, HYH Wong, GCY Chan, YKK Lee, CP Tang, MHY Ng, EHY Kan, ASY	2020
	Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong Journal:Journal of Obstetrics and Gynaecology Research	So, PL Cheng, YKY Cheuk, KY Chiu, WK Mak, SL Mok, SL Lo, TK Yung, WK Lo, FM Chung, BHY Kan, SYA Lee, CP Tang, MHY	2017
	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
	An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations Journal:Hemoglobin	Lee, HLH Mak, ASL Kou, KOT Poon, CF Wong, WS Chiu, KH Au, HHL Chan, YK Kan, SYA Tang, MHY Leung, KY	2016
	Next generation sequencing in prenatal diagnosis Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017	Leung, GKC Mak, CCY Pei, SLC Tsang, MHY Yu, MHC Yeung, KS Mok, GTK Hui, APW Tang, MHY Chan, KYK Kan, SYA Chung, BHY	2017
	Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016
	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
	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
	Homozygous Missense Mutation in ABR Causes Cerebellar Hypoplasia with Early Lethality - A New Condition Identified by Exome Sequencing? Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Ying, D Shek, NWM Chu, WY Yeung, KS Leung, KC Tang, MHY Kan, SYA Chan, YK Chung, BHY	2014
	Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma dna sequencing Journal:PLoS ONE	Chen, EZ Chiu, RWK Sun, H Akolekar, R Chan, KCA Leung, TY Jiang, P Zheng, YWL Lun, FMF Chan, LYS Jin, Y Go, ATJI Lau, ET To, WWK Leung, WC Tang, RYK AuYeung, SKC Lam, H Kung, YY Zhang, X van Vugt, JMG Minekawa, R Tang, MHY Wang, J Oudejans, CBM Lau, TK Nicolaides, KH Lo, YMD	2011
	Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome Journal:Prenatal Diagnosis	Au, PKC Kwok, YKY Leung, KY Tang, LYF Tang, MHY Lau, ET	2011
	Simultaneous real-time imaging of four-chamber and left ventricular outflow tract views using xPlane imaging capability of a matrix array probe Journal:Ultrasound in Obstetrics and Gynecology	Yuan, Y Leung, KY Ouyang, YS Yang, F Tang, MHY Chau, AKT Dai, Q	2011
	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
	Homozygous missense mutation in ABR causes cerebellar hypoplasia with early lethality: a new condition identified by exome sequencing? Proceeding/Conference:American Journal of Medical Genetics Part A	Ying, D Shek, NWM Chu, YWY Yeung, KS Leung, KC Tang, MHY Kan, ASY Chan, YK Chung, BHY	2015
	Identifying genetic mutations in patients with Rasopathies using a Next Generation Sequencing Diagnostic Pipeline in Hong Kong Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Lo, IFM Leung, KC Luk, HM Tang, VHM Gao, W Wong, WL Tang, LYF Chu, WY Kan, SYA Tang, MHY Lam, STS Yang, W Ma, CH Jin, D Chan, YK Chung, BHY	2014
	Integration of chromosomal microarray into paediatric clinical care in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2013	Tao, V Chu, YWY Chan, KY Lau, EYL Mok, GTK Tso, W Liu, A Kan, A Tang, MH Lau, YL Chung, BHY	2013
	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
	Chinese fetal renal pelvis-measurements at 12-14 weeks of gestation Proceeding/Conference:International Scientific Meeting of the International Society of Ultrasound in Obstetrics and Gynecology, ISUOG 2007	Chen, M Lee, CP Lam, YH Chan, JSM Tang, MHY	2007
	Massive parallel sequencing for the genetic diagnosis of rasopathies: a study of 58 Chinese patients in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2013	Lo, IFM Leung, KC Luk, MHM Wong, WL Tang, LYF Chu, YWY Kan, ASY Tang, MHY Lam, STS Yang, W Chan, YK Chung, BHY	2013
	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