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Title	Author(s)	Issue Date	Views
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
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
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
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
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
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
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
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
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	188
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	194
Replicative MCM7 protein as a proliferation marker in endometrial carcinoma: A tissue microarray and clinicopathological analysis Journal:Histopathology	Li, SS Xue, WC Khoo, US Ngan, HYS Chan, KYK Tam, IYS Chiu, PM Ip, PPC Tam, KF Cheung, ANY	2005	136
Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population. Journal:Human mutation	Khoo, US Chan, KY Cheung, AN Xue, WC Shen, DH Fung, KY Ngan, HY Choy, KW Pang, CP Poon, CS Poon, AY Ozcelik, H	2002	173
Promoter methylation of death-associated protein kinase and its role in irradiation response in cervical cancer Journal:Oncology Reports	Leung, RCY Liu, SS Chan, KYK Tam, KF Chan, KL Wong, LC Ngan, HYS	2008
Promoter methylation and differential expression of π-class glutathione S-transferase in endometrial carcinoma Journal:Journal of Molecular Diagnostics	Chan, QKY Khoo, US Chan, KYK Ngan, HYS Li, SS Chiu, PM Man, LS Ip, PPC Xue, WC Cheung, ANY	2005	121
Promoter hypermethylation of multiple genes in hydatidiform mole and choriocarcinoma Journal:Journal of Molecular Diagnostics	Xue, WC Chan, KYK Feng, HC Chiu, PM Ngan, HYS Tsao, SW Cheung, ANY	2004	92
Primary peritoneal malignant mixed mfcllerian tumors: A clinicopathologic, immunohistochemical, and genetic study Journal:Cancer	Shen, DH Khoo, US Xue, W Ngan, HYS Wang, JL Liu, VWS Chan, YK Cheung, ANY	2001	172
Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications Journal:American Journal of Medical Genetics Part A	Yu, PT Shu, W Mok, SL Hui, PW Chan, LW Kwok, KY Chan, YK Lo, TK Chung, BHY Luk, HM Kan, SYA	2022	9
Prenatal diagnosis of familial atretic encephalocele Journal:Ultrasound in Obstetrics and Gynecology	Lau, WL Yung, WY Leung, WC Kan, A Chan, K Luk, HM Kan, E Lam, YY	2019
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 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

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