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Showing results 13 to 32 of 34 < previous next >

Title	Author(s)	Issue Date	Views
Evaluation of aCGH for prenatal diagnosis Proceeding/Conference:Roche Applied Science User Conference 2011	Lau, ETK	2011
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	32
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
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
Findings on Prenatal aCGH evaluation Proceeding/Conference:33rd Fetoscopy Working Group Meeting 2011	Lau, ETK	2011	25
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	69
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	207
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	95
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	88
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
Prenatal diagnostic service - present Proceeding/Conference:30 years of Medical Genetics in Hong Kong	Lau, ETK	2011	21
Principle and diagnostic pitfall of PCR and FISH Proceeding/Conference:HA Commissioned Training in O&G. February 28, 2011, Hong Kong.	Lau, ETK	2011	25
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	76
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	124
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	48
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	108
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	29
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	45
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	181

Showing results 13 to 32 of 34 < previous next >