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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date
	13q - In a fetus with ultrasonographic diagnosis of exencephaly in the first trimester [2] Journal:Prenatal Diagnosis	Lam, YH Tang, MHY Ng, LKL	1998
	Absence of microdeletion and common mutation in 13q32 in a balanced translocation with holoprosencephaly Proceeding/Conference:3rd Hong Kong Medical Genetics Conference	Wong, KM Tang, LYF Kwok, KY Yu, DL Ng, LKL Lee, CP Lo, S Tang, MHY Lau, ET	2005
	Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong Journal:Hong Kong Medical Journal	Ng, PPY Tang, MHY Lau, ET Ng, LKL Ng, EHY Tam, PC Yeung, WSB Ho, PC	2009
	Chronosome anomalies and Y-microdeletions in subfertile men Proceeding/Conference:ACGA-HKSMG 2008 International Conference	Ng, PPY Tang, MHY Lau, ET Ng, LKL Ng, EHY Tam, PC Yeung, WSB Ho, PC	2008
	Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong Journal:Prenatal Diagnosis	Leung, KY Lee, CP Tang, MHY Lau, ET Ng, LKL Lee, YP Chan, HY Ma, ESK Chan, V	2004
	First-trimester ultrasound diagnosis of holoprosencephaly: Three case reports Journal:Ultrasound in Obstetrics and Gynecology	Wong, HS Lam, YH Tang, MHY Cheung, LWK Ng, LKL Yan, KW	1999
	Full karyotyping, rapid aneuploidy diagnosis or both when invasive prenatal testing is performed for diagnosis of thalassaemia? Journal:Molecular Human Reproduction	Tse, KY Leung, WC Leung, KY Lee, CP Ng, LKL Lau, ET Chan, V Tang, MHY	2006
	De Novo Euchromatic band within qh region of chromosome 9 Proceeding/Conference:3rd Hong Kong Medical Genetics Conference	Tam, WK Kwok, KY Ng, LKL Chan, WK Chan, SSY Lau, ET Tang, MHY	2005
	Prenatal detection of a de novo Yqh-acrocentric translocation Journal:Clinical Biochemistry	Ng, LKL Kwok, YK Tang, LYF Ng, PPY Ghosh, A Lau, ET Tang, MHY	2006
	Prenatal detection of an unbalanced Yqh-Acrocentric translocation Proceeding/Conference:3rd Hong Kong Medical Genetics Conference	Ng, LKL Kwok, KY Tang, LYF Ng, PPY Ghosh, A Lau, ET Tang, MHY	2005
	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
	Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: What would be missed, who should decide? Journal:Hong Kong Medical Journal	Leung, WC Lau, ET Lau, WL Tang, R Wong, SF Lau, TK Tse, KT Wong, SF To, WK Ng, LKL Lao, TT Tang, MHY	2008
	Risk of fetal aneuploidy and feasibility of rapid aneuploidy screening in thalassaemia couples Proceeding/Conference:British Congress of Obstetrics & Gynaecology Meeting	Tse, KY Leung, WC Leung, KY Lee, CP Ng, LKL Lau, ET Chan, VNY Tang, MHY	2004
	Robertsonian translocations (21;21) and (13;13) may not be detected by fluorescence in situ hybridization in uncultured fetal lymphocytes Proceeding/Conference:2nd Hong Kong Medical Genetics Conference	Kwok, YK Lau, ET Hsu, BP Ng, LKL Tang, MHY	1999

Showing results 1 to 14 of 14