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Title	Author(s)	Issue Date	Views
22q11.2 deletion syndrome in adult Chinese Patients with Conotruncal Anomalies: dysmorphisms, clinical features and underdiagnosis Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Liu, APY Chow, PC Lee, PPW Mok, TKG Tang, WF Lau, ETK Lam, STS Chan, KY Kan, SYA Chau, AKT Cheung, YF Lau, YL Chung, BHY	2013	115
A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin Journal:Journal of Obstetrics and Gynaecology Research	Kan, SYA Lau, ETK So, CH Chan, WP Wong, WC Lee, KC Pertile, MD Tang, MHY	2018	38
A fetus with Hb Bart’s disease due to maternal uniparental disomy for chromosome 16 Journal:Hemoglobin	Au, PK Kan, ASY Tang, MHY Leung, KY Chan, KY Tang, TW Lau, ETK	2016	79
Alport's syndrome: case of a giant esophageal tumor Journal:Esophagus	Tsang, JS Tong, DKH Chung, BHY Tang, MHY Lau, ETK Chan, GCF Law, SYK	2013	79
Application of rapid aneuploidy detection versus karyotyping in prenatal diagnosis Journal:Chinese Journal of Obstetrics and Gynaecology	Leung, WC Chen, M Lau, ETK Lao, TTH Tang, MHY	2007	97
Automating non-invasive prenatal diagnosis of HB Barts disease on immunofluorescence staining of fetal erythrocytes in maternal blood Proceeding/Conference:International Conference on Prenatal Diagnosis & Therapy, ISPD 2006	Lau, ETK Kwok, KY Leung, KY Tang, MHY	2006	45
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	101
Confined placental mosaicism of trisomy 16 presenting with placental mass and intrauterine death Proceeding/Conference:International Scientific Meeting of the International Society of Ultrasound in Obstetrics and Gynecology, ISUOG 2007	Hui, PW Leung, KY Lau, ETK Tang, MHY	2007	129
Copy number variation in Hong Kong patients with autism spectrum disorder Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Mak, ASL Leung, GKC Mak, CCY Chu, YWY Mok, GTK Tang, TWF Chan, KYK Kan, ASY Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, VCN Lee, SL Chung, BHY	2016	113
Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong Journal:Clinical and Translational Medicine	Siu, CWK Lam, CW Mak, CM Lau, ETK Tang, MHY Tang, WF Poon-Mak, RS Lee, CC Hung, SF Leung, PW Kwong, KL Yau, EK Ng, GS Fong, NC Chan, KY	2016	94
Disclosing results of autism genomic testing-systematic review and applying its results to clinical practice Proceeding/Conference:International Meeting for Autism Research, IMFAR 2012	Chung, B Cheuk, DKL Tang, M Lau, ETK Chan, YK Lau, YL	2012	111
Evaluation of aCGH for Prenatal Diagnosis Proceeding/Conference:Prenatal Diagnosis Conference (全国产前诊断暨产前超声新技术新进展学习班)	Lau, ETK	2011	41
Evaluation of aCGH for prenatal diagnosis Proceeding/Conference:Roche Applied Science User Conference 2011	Lau, ETK	2011	23
Evidence of spread of X Chromosome inactivation on Chromosome 15 in a girl with an Unbalanced t(X;15) Translocation Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Yeung, KS Chee, WYY Luk, HM Tang, MHY Lau, ETK Shuen, YA Lo, IFM Chan, YK Chung, BHY	2013	76
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	106
Findings on Prenatal aCGH evaluation Proceeding/Conference:33rd Fetoscopy Working Group Meeting 2011	Lau, ETK	2011	31
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care Proceeding/Conference:European Journal of Human Genetics	Chung, B Chow, P Liu, A Lee, P Wong, V Chan, K Tang, M Lun, KS Lau, ETK Cheung, YF Chau, KT Lau, YL	2013	99
Maternal serum anti-Mullerian hormone level is not superior to chronological age in predicting down syndrome pregnancies Journal:Prenatal Diagnosis	Li, HWR Hui, PW Tang, MHY Lau, ETK Yeung, WSB Ho, PC Ng, EHY	2010	231
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	100
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	90

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