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	Title	Author(s)	Issue Date	Views
	Letters to the editor Journal:Contraception	Soderstrom, RM Kan, ASY Ng, EHY Pak, CH	2005	31
	Massive parallel sequencing for the genetic diagnosis of rasopathies: a study of 58 Chinese patients in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2013	Lo, IFM Leung, KC Luk, MHM Wong, WL Tang, LYF Chu, YWY Kan, ASY Tang, MHY Lam, STS Yang, W Chan, YK Chung, BHY	2013	48
	Outcome of twin pregnancies after amniocentesis Journal:Journal of Obstetrics and Gynaecology Research	Kan, ASY Lee, CP Leung, KY Chan, BCP Tang, MHY Chan, VHY	2012	56
	Pain control in first-trimester suction evacuation Journal:IPPF Medical Bulletin	Kan, ASY Ho, PC	2006	85
	Pattern and predictors of medical care received by hepatitis B carriers during pregnancy and after delivery Journal:Public Health	Cheung, KW Seto, MTY Wong, D Mak, ASL So, PL Lau, WL Wang, W Kan, ASY Lee, CP Ng, EHY	2019
	Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature Journal:American Journal of Medical Genetics Part A	Seto, MTY Bertoli-Avella, AM Cheung, KW Chan, KYK Yeung, KS Fung, JLF Beetz, C Bauer, P Luk, HM Lo, IFM Lee, CP Chung, BHY Kan, ASY	2021	18
	Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis Journal:Clinical Case Reports	LIN, SM LUK, HM LO, IFM TAM, WK Chan, KYK TSE, HY Leung, WC Tang, MHY Kan, ASY	2020	13
	Prenatal diagnosis of 5p deletion syndrome: Report of five cases Journal:Journal of Obstetrics and Gynaecology Research	Mak, ASL Ma, TWL Chan, KYK Kan, ASY Tang, MHY Leung, KY	2019	28
	Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in <i>SMAD4</i> gene presented with thick nuchal translucency and cardiac abnormalities Journal:Prenatal Diagnosis	Hui, PW Mok, YK Luk, HM Au, SLK Lau, EYT Chung, B Kan, ASY	2-Aug-2023
	Prevalence of chlamydia trachomatis infection in subfertile women in Hong Kong Journal:Hong Kong Journal of Gynaecology, Obstetrics and Midwifery	Kan, ASY Ng, EHY Ho, PC	2002	90
	A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12-20 weeks gestation Proceeding/Conference:Meeting of the American Society of Reproductive Medicine, ASRM 2005	Tang, FOS Chan, CCW Kan, ASY Ho, PC	2005
	A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12-20 weeks gestation Journal:Human Reproduction	Tang, OS Chan, CCW Kan, ASY Ho, PC	2005	52
	The role and comparison of two techniques of paracervical block for pain relief during suction evacuation for first-trimester pregnancy termination Journal:Contraception	Kan, ASY Ng, EHY Ho, PC	2004
	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
	The effect of rupture of membranes and labour on the risk of hepatitis B vertical transmission: Prospective multicentre observational study Journal:European Journal of Obstetrics & Gynecology and Reproductive Biology	Cheung, KW Seto, MTY So, PL Wong, D Mak, ASL Lau, WL Wang, W Kan, ASY Lee, CP Ng, EHY	2019
	The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine	Yeung, KS Yu, FNY Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Leung, KY Chung, WH Lee, YT Ng, VKS YU, HC Fung, JLF TSANG, MHY Chan, KYK Chan, SHS Kan, ASY Chung, BHY	2020	49
	Updates on Screening for Carriers of Genetic Diseases Journal:Journal of Paediatrics, Obstetrics and Gynaecology	Cheng, HHY Kan, ASY	2018	28
	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
	An X-linked dominant mutation in LAMP2 causing Danon disease associated with myotonia expanding the spectrum Proceeding/Conference:Neuromuscular Disorders	Chan, SHS Kan, ASY Tse, HF	2013	48

Showing results 19 to 37 of 37 < previous