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Showing results 1 to 7 of 7

	Title	Author(s)	Issue Date	Views
	A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report Journal:Diagnostics	Ng, KSV Lau, TK Kan, SYA Chung, BHY Luk, HM Ng, WF Shi, M Choy, KW Cao, Y Leung, WC	2021	4
	First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing Journal:Genes	Shu, W Cheng, SS.W.Xue, S Chan, LW Soong, SI Kan, SYA Cheung, SWH Choy, KW	2021	4
	Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies Journal:Genes	So, PL Hui, AST Ma, TWL Shu, W Hui, PW Kong, CW Lo, TK Kan, ABC Kan, EYL Chong, SC Chung, BHY Luk, HM Choy, KW Kan, SYA Leung, WC	2022
	Monozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3 Journal:Fetal Diagnosis and Therapy	Leung, WC Choi, H Lau, WL Ng, LK Lau, ET Lo, FM Choy, KW Lau, TK Tang, MHY Chin, R	2009	85
	Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH Journal:Journal of Maternal-Fetal and Neonatal Medicine	Choy, KW Chan, LW Tang, MHY Ng, LKL Leung, TY Lau, TK	2009	96
	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
	Recurrent BRCA2 mutation is found in Chinese ovarian cancer patients Proceeding/Conference:HKICC / RPS 2000	Fung, KY Chan, YK Poon, AYA Cheung, ANY Ngan, HYS Choy, KW Pang, CP Poon, CSP Khoo, US	2000

Showing results 1 to 7 of 7