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Title	Author(s)	Issue Date	Views
c-mos Immunoreactivity Aids in the Diagnosis of Gestational Trophoblastic Lesions Journal:International Journal of Gynecological Pathology	Xue, WC Khoo, US Ngan, HYS Chan, KYK Ip, PPC Tsao, SW Cheung, ANY	2004	251
Caspase activity is downregulated in choriocarcinoma: A cDNA array differential expression study Journal:Journal of Clinical Pathology	Fong, PY Xue, WC Ngan, HYS Chiu, PM Chan, KYK Tsao, SW Cheung, ANY	2006
Category ‐ Maternal Medicine Journal:BJOG: An International Journal of Obstetrics & Gynaecology	Hui, PW Ma, WLT Chan, SSY Cheung, KW Lai, FKY Ho, SKD Chan, YK	2022
The CD209 (DC-SIGN) -336A>G and MxA -123C>A promoter polymorphisms in severe acute respiratory syndrome coronavirus infection in Hong Kong Chinese Proceeding/Conference:Health Research Symposium	Khoo, US Chan, KYK Ching, JCY Xu, MS So, KM Lai, ST Chu, CM Yam, L Wong, TY Chung, PH Chan, VSF Tam, P Yip, SP Lin, CL Sham, P Leung, GM Peiris, JSM	2010	151
CD209 (DC-SIGN) -336A>G promoter polymorphism and severe acute respiratory syndrome in Hong Kong Chinese Journal:Human Immunology	Chan, KYK Xu, MS Ching, JCY So, TMK Lai, ST Chu, CM Yam, LYC Wong, ATY Chung, PH Chan, VSF Lin, CLS Sham, PC Leung, GM Peiris, JSM Khoo, US	2010	217
Cervical Cytology Screening in Pregnant Women Proceeding/Conference:HKICC / RCC 2006	Tsun, OKL Yeung, YH Chan, YK Siu, KY Szeto, EF Chan, KYQ Chan, KW Cheung, ANY	2006	103
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis Journal:Molecular Genetics & Genomic Medicine	LEUNG, KC Ying, D MAK, CCY Chen, XY Xu, W YEUNG, KS Wong, WL Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Sham, PC Lau, YL Chung, BHY Lee, SL	2017	110
CFTR: p.I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with Cystic Fibrosis Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014	Chung, BHY Leung, KC Mak, CCY Chow, CSK Ying, JD Chu, YWY Yang, WL Lau, YL Chan, KYK Lee, SL	2014
Characterization of the pathogenic mechanism of a novel BRCA2 variant in a Chinese family Journal:Familial Cancer	Kwong, A Wong, LP Chan, KYK Ma, ESK Khoo, US Ford, JM	2008
Chinese patients with rasopathies: Detection of 29 known and novel variants using next-generation sequencing (NGS) Proceeding/Conference:36th Annual David W. Smith Workshop	Leung, KC Lo, I Luk, HM Tang, HMV Gao, W Wong, WL Chu, WY Lam, STS Ma, CH Jin, D Chan, YK Chung, BHY	2015	50
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
Clinical implications of large rare copy number variations in 110 Chinese patients with conotruncal heart disease Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014	Mak, CCY Chow, PC Chau, AKT Chan, YK Bassett, AS Chung, BHY	2014	48
Clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in genetic diseases 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	Yu, MHC Au, LKS Chan, YK Tang, MHY Kan, SYA Chung, BHY	2019
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism Journal:International Journal of Pediatric Endocrinology	Tung, JYL Lai, SHY Au, SLK Yeung, KS Kan, ASY Loong, F DeLeon, DD Kalish, JM Ganguly, A Chung, BHY Chan, KYK	2020
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese Journal:npj Genomic Medicine	Chau, FTJ YU, HC Chui, MCM Yeung, CCW Kwok, AWC ZHUANG, X Lee, R Fung, LF LEE, M Mak, CCY Ng, YTN Chung, CY Chung, CY TSANG, HY Chan, JCK Chan, YK Kan, ASY Chung, HY Yang, W Lee, SL Chan, GCF Tam, PKH Lau, YL Yeung, KS Chung, BHY Tang, SM	2022	12
Constitutively nuclear FOXO3a localization predicts poor survival and promotes Akt phosphorylation in breast cancer Journal:PLoS ONE	Chen, J Gomes, AR Monteiro, LJ Wong, SY Wu, LH Ng, TT Karadedou, CT Millour, J Ip, YC Cheung, YN Sunters, A Chan, KYK Lam, EWF Khoo, US	2010	240
Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong Journal:BMC Pregnancy and Childbirth	CHUNG, CCY Chan, KYK Hui, PW Au, PKC Tam, WK Li, SKM Leung, GKC Fung, JLF Chan, MCY Luk, HM Mak, ASL Leung, KY Tang, MHY Chung, BHY Kan, ASY	2020	44
Cryptic 12q duplication: a case study Proceeding/Conference:1st BCM-CUHK (Baylor College of Medicine-The Chinese University of Hong Kong) Joint Symposium in Clinical Genetics and Birth Defects, 2017	Lam, OM Tam, WK Tang, YF Li, KM Chan, YK Kan, SYA	2017	27
DC-SIGN and L-SIGN: The SIGNs for infection Journal:Journal of Molecular Medicine	Khoo, US Chan, KYK Chan, VSF Lin, CLS	2008
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine	MAK, CCY Chow, PC Liu, APY Chan, YK Chu, WY Mok, TKG LEUNG, KC YEUNG, KS Chau, AKT Lowther, C Scherer, SW Marshall, CR Bassett, AS Chung, BHY	2016	90

Showing results 12 to 31 of 181 < previous next >