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Showing results 51 to 61 of 61 < previous

	Title	Author(s)	Issue Date	Views
	Study of the extent of information desired by women undergoing non-invasive prenatal testing following positive prenatal Down-syndrome screening test results Journal:International Journal of Gynecology & Obstetrics	Lo, TK Chan, YK Kan, SYA So, PL Kong, CW Mak, SL Lee, CN	2017	39
	The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8 Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing	Yeung, KS Yu, YN Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Yu, MHC Fung, JLF Tsang, MHY Chan, YK Chan, HSS Kan, SYA Chung, BHY	2019	36
	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	39
	Two unusual cases of haemoglobin Bart’s hydrops fetalis screened negative on universal prenatal screening for thalassaemia Proceeding/Conference:Ultrasound in Obstetrics and Gynecology	Kou, KO Lee, HH Lau, B Wong, WS Kan, SYA Tang, MHY Poon, CF Leung, KY	2013	95
	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	88
	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	37
	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	61
	What is the Diagnosis? Journal:Hong Kong Journal of Paediatrics (New series)	Chiu, TA Chu, WY Kan, SYA Chung, BHY	2016	32
	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	82
	Women’s stated test preference on questionnaire versus their actual choice in real clinical setting regarding non-invasive prenatal test Journal:European Journal of Obstetrics & Gynecology and Reproductive Biology	Lo, TK Chan, YK Kan, SYA So, PL Kong, CW Mak, SL Lee, CN	2017	25

Showing results 51 to 61 of 61 < previous