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Showing results 1 to 18 of 18

	Title	Author(s)	Issue Date
	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
	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
	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
	Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory Journal:Healthcare	Lai, HTT Lau, ETK Lau, YTE Lo, HM Chan, YK Cheung, KW Ma, TWL Leung, WC Kong, CW Shu, W So, PL Kwong, KY Mak, CCY Lee, M Chui, MCM Chung, BHY Kan, SYA	2022
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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
	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

Showing results 1 to 18 of 18