Browsing by Author Ng, LKL

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TitleAuthor(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, KMTang, LYFKwok, KYYu, DLNg, LKLLee, CPLo, STang, MHYLau, ET
2005
 
Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong
Journal:Hong Kong Medical Journal
Ng, PPYTang, MHYLau, ETNg, LKLNg, EHYTam, PCYeung, WSBHo, PC
2009
 
Cost-effectiveness of prenatal screening for thalassaemia in Hong Kong
Journal:Prenatal Diagnosis
Leung, KYLee, CPTang, MHYLau, ETNg, LKLLee, YPChan, HYMa, ESKChan, V
2004
 
First-trimester ultrasound diagnosis of holoprosencephaly: Three case reports
Journal:Ultrasound in Obstetrics and Gynecology
Wong, HSLam, YHTang, MHYCheung, LWKNg, LKLYan, KW
1999
 
De Novo Euchromatic band within qh region of chromosome 9
Proceeding/Conference:3rd Hong Kong Medical Genetics Conference
Tam, WKKwok, KYNg, LKLChan, WKChan, SSYLau, ETTang, MHY
2005
 
Prenatal detection of a de novo Yqh-acrocentric translocation
Journal:Clinical Biochemistry
Ng, LKLKwok, YKTang, LYFNg, PPYGhosh, ALau, ETTang, MHY
2006
 
Prenatal detection of an unbalanced Yqh-Acrocentric translocation
Proceeding/Conference:3rd Hong Kong Medical Genetics Conference
Ng, LKLKwok, KYTang, LYFNg, PPYGhosh, ALau, ETTang, MHY
2005
 
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, YKLau, ETHsu, BPNg, LKLTang, MHY
1999
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