Browsing by Author Yeung, KS

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Showing results 68 to 78 of 78 < previous 
TitleAuthor(s)Issue DateViews
 
Silver-Russell syndrome in Hong Kong
Journal:Hong Kong Medical Journal
Luk, HMYEUNG, KSWong, WLChung, BHYTong, TMFLo, IFM
2016
62
 
Somatic mosaicism of PIK3CA mutation in PIK3CA-related overgrowth disorders
Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014
Yeung, KSLeung, KCWong, WLLi, RCHChoi, KYKuong, EYLChow, WTo, MChan, GCFChung, BHY
2014
72
 
Somatic PIK3CA mutations in seven patients with PIK3CA-related overgrowth spectrum
Journal:American Journal of Medical Genetics Part A
YEUNG, KSIp, JKJChow, CPKuong, EEYLTam, PKHChan, GCFChung, BHY
2017
 
Spread of X Inactivation on Chromosome 15 is Associated with a More Severe Phenotype in a Girl with an Unbalanced t(X;15) Translocation
Journal:American Journal of Medical Genetics Part A
Yeung, KSChee, WYYLuk, HMKan, ASYTang, MHYLau, ETKShuen, AYLo, IFMChan, YKChung, BHY
2014
76
 
A study of the non-legal factors that may affect the quantum of land compensation in the Lands Tribunal in Hong Kong
Journal:Facilities
Leung, HFYeung, KS
2008
82
 
Surgical Vision: Google Glass and Surgery
Journal:Surgical Innovation
Chang, JYTsui, LYYeung, KSYip, SWLeung, GKK
2016
45
 
Synthesis and molecular structures of novel seven-co-ordinated oxo- and nitrido-rhenium(V) complexes of 2,2′:6′,2″:6″,2‴-quaterpyridine
Journal:Journal of the Chemical Society, Dalton Transactions
Che, CMWang, YPYeung, KSWong, KYPeng, SM
1992
60
 
The genetics of macrocephaly, autistic spectrum disorders and developmental delay in Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
Tso, WYWYEUNG, KSIp, JKJLiu, APYLee, PPWChu, WYChong, CYHo, MHKChan, GCFLau, YLChung, BHY
2017
161
 
The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes
Journal:Molecular Genetics & Genomic Medicine
Yeung, KSYu, FNYFung, CWWong, SLee, HCHFung, STHFung, GPGLeung, KYChung, WHLee, YTNg, VKSYU, HCFung, JLFTSANG, MHYChan, KYKChan, SHSKan, ASYChung, BHY
2020
49
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
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
Yeung, KSYu, YNFung, CWWong, SLee, HCHFung, STHFung, GPGYu, MHCFung, JLFTsang, MHYChan, YKChan, HSSKan, SYAChung, BHY
2019
 
X-ray structure and spectroscopic properties of platinum(II) complexes of 1,1′-biisoquinoline
Journal:Polyhedron
Cheng, LKYeung, KSChe, CMCheng, MCWang, Y
1993
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