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Showing results 1 to 7 of 7

	Title	Author(s)	Issue Date
	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
	Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome Journal:Prenatal Diagnosis	Au, PKC Kwok, YKY Leung, KY Tang, LYF Tang, MHY Lau, ET	2011
	Identifying genetic mutations in patients with Rasopathies using a Next Generation Sequencing Diagnostic Pipeline in Hong Kong Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Lo, IFM Leung, KC Luk, HM Tang, VHM Gao, W Wong, WL Tang, LYF Chu, WY Kan, SYA Tang, MHY Lam, STS Yang, W Ma, CH Jin, D Chan, YK Chung, BHY	2014
	Massive parallel sequencing for the genetic diagnosis of rasopathies: a study of 58 Chinese patients in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2013	Lo, IFM Leung, KC Luk, MHM Wong, WL Tang, LYF Chu, YWY Kan, ASY Tang, MHY Lam, STS Yang, W Chan, YK Chung, BHY	2013
	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 screening for 22q11.2 microdeletion in fetuses with congenital heart defects Proceeding/Conference:3rd Hong Kong Medical Genetics Conference	Tang, LYF Kwok, KY Fung, QLS Tang, MHY Lau, ET	2005

Showing results 1 to 7 of 7