Browsing by Author YU, HC

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Showing results 23 to 26 of 26 < previous 
TitleAuthor(s)Issue DateViews
 
Reanalyzing clinical whole exome sequencing (WES) data aprovides additional diagnosis in paediatric-onset undiagnosed diseases – a Yale-HKU collaborative study
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
Fung, LFHuang, SPajusalu, SYu, HCChan, MMak, CHui, VChung, CYLek, MChung, BHY
2019
59
 
Reanalyzing clinical whole exome sequencing (WES) data provides additional diagnosis in paediatric-onset undiagnowed diseases – A Yale-HKU collaboration
Proceeding/Conference:Asia-Pacific Conference on Human Genetics (APCHG) 2019
Fung, LFHuang, SPajusalu, SYU, HCChan, MLek, MChung, BHY
2019
30
 
Speech intelligibility using various cochlear implant speech coding strategies
Proceeding/Conference:Proceedings of the 5th Asia Pacific Symposium on Cochlear Implant and Related Sciences : Hong Kong, November 26 - 28, 2005
Wong, LLNCiocca, VVandali, AELuk, BIp, VWKMurray, BYu, HCChung, I
2005
79
 
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
Showing results 23 to 26 of 26 < previous