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Showing results 1 to 14 of 14

	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
	Array CGH evaluation for prenatal diagnosis in Hong Kong Proceeding/Conference:Prenatal Diagnosis	Lau, ET Tang, WF Chan, SY Ding, CK Kan, ASY Lee, CP Hui, PW Leung, KY Ma, T Leung, WC Tang, MHY	2012	181
	Array CGH testing in prenatal diagnosis: a promising new service with improved diagnostic yield and shortened reporting time Proceeding/Conference:Hospital Authority Convention, HAC 2012	Kan, ASY Lau, ET Tang, WF Chan, SY Ding, CK Lee, CP Hui, PW Leung, KY Ma, T Leung, WC Chan, YK Tang, MHY	2012
	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	87
	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	88
	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
	A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - Is cardiac assessment necessary for all patients with 17p13.3 microduplication? Journal:European Journal of Medical Genetics	Ho, ACC Liu, APY Lun, KS Tang, WF Chan, KYK Lau, EYT Tang, MHY Tan, TY Chung, BHY	2012	89
	Next-generation sequencing with a 54-gene panel identified unique mutational profile and prognostic markers in Chinese patients with myelofibrosis Journal:Annals of Hematology	Singh, GHH Ip, HW Yim, RLH Tang, WF Pang, HMH Lee, P Leung, GMK Li, JWY Tang, K So, JCC Leung, RYY Li, J Panagiotou, I Lam, CCK Kwong, YL	2019	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
	Redefining prognostication of de novo cytogenetically normal acute myeloid leukemia in young adults Journal:Blood Cancer Journal	Tsui, SP Ip, HW Saw, NY Zhang, C Cheung, AK Ng, NK Man, CH Lam, SS Tang, WF Lin, CH Cheng, GH Au, CH Ma, ES Chan, TL So, JC Ng, MH Cheng, KC Wong, KF Siu, LP Yip, SF Lin, SY Lau, JS Luk, TH Lee, HK Lau, CK Kho, B Sim, JP Kwong, YL Leung, SY Javed, A Leung, AY	2020	111
	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
	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
	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	84
	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	95

Showing results 1 to 14 of 14