Showing results 23 to 34 of 34
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine | 2020 | 19 | ||
New cochlear implant coding strategy for tonal language speakers Journal:International Journal of Audiology | 2008 | 78 | ||
Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020 | 2020 | 11 | ||
| 2018 | 124 | |||
Pitch and tonal language perception in cochlear implant users Proceeding/Conference:The 2007 Conference on Implantable Auditory Prostheses | 2007 | 101 | ||
Pitch perception by cochlear implants users Proceeding/Conference:Proceedings of the 5th Asia Pacific Symposium on Cochlear Implant and Related Sciences : Hong Kong, November 26 - 28, 2005 | 2005 | 120 | ||
| 1989 | 177 | |||
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 | 2019 | 30 | ||
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 | 2019 | 23 | ||
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 | 2005 | 91 | ||
TGM6 variants in Chinese population – is it disease causing? Proceeding/Conference:2nd Joint Annual Research & Scientific Meeting 2018 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association and Hong Kong College of Paediatric Nursing | 2018 | 36 | ||
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 | 2020 | 35 |