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Title	Author(s)	Issue Date
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
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
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
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
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
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
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
The tandem repeat polymorphism of the DC-SIGNR gene is associated with susceptibility to SARS coronavirus infection in Chinese from Hong Kong Proceeding/Conference:HUGO annual Human Genome Meeting, HGM 2004	Khoo, US Chan, KYK Yip, VSP Peiris, JSM Tin, V Liu, W Xue, W Ngan, HYS Chan, LC Cheung, ANY	2004
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
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
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
Study of human papillomavirus status in Southern Chinese women with normal cervix, precancerous cervical lesions and cervical cancers Proceeding/Conference:Health Research Symposium	Ngan, HYS Liu, S Leung, TW Cheung, ANY Chan, YK	2007
Stem cell related genes and malignant progression in gestational trophoblastic diseases Proceeding/Conference:Cancer Research	Cheung, ANY Chiu, PM Chan, QKY Chan, YK Ngan, HYS	2005
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
Single nucleotide polymorphisms of follicle-stimulating hormone receptor are associated with ovarian cancer susceptibility Journal:Carcinogenesis	Yang, CQ Chan, KYK Ngan, HYS Khoo, US Chiu, PM Chan, QKY Xue, WC Cheung, ANY	2006
Single nucleotide polymorphisms (SNPs) in the coding sequence of follicle stimulating hormone receptor (FSHR) are associated with ovarian cancer susceptibility Proceeding/Conference:Cancer Research	Yang, C Ngan, HYS Khoo, US Chan, YK Chiu, PM Chan, QKY Xue, W Cheung, ANY	2004
Single nucleotide polymorphism of Pi-class glutathione S-transferase and susceptibility to endometrial carcinoma Journal:Clinical Cancer Research	Chan, QKY Khoo, US Ngan, HYS Yang, CQ Xue, WC Chan, KYK Chiu, PM Ip, PPC Cheung, ANY	2005
Single nucleotide polymorphism of metabolizing enzymes is associated with risk of ovarian carcinoma in Chinese women Proceeding/Conference:International Meeting on Human Genome Variation & Complex Genome Analysis, HGV 2006	Chan, KYQ Ngan, HYS Chan, YK Siu, KY Chiu, PM Khoo, US Ip, PPC Cheung, ANY	2006
Significance of single nucleotide polymorphism of the metabolizing enzyme NQO1 in ovarian cancer – a sequenom and clinicopathologic study on Chinese women Proceeding/Conference:Research Postgraduate Symposium, RPS 2006	Chan, KYQ Ngan, HYS Chan, YK Siu, KY Chiu, PM Khoo, US Ip, PPC Cheung, ANY	2006
Screening for recurrent BRCA1 mutations in Chinese ovarian cancer Proceeding/Conference:Biennial Meeting of the International Gynecologic Cancer Society, IGCS 1999	Khoo, US Cheung, ANY Ngan, HYS Chan, KYK Ozcelik, H	1999

Showing results 1 to 20 of 129 next >