Showing results 18 to 26 of 26
< previous
Title | Author(s) | Issue Date | |
---|---|---|---|
New cochlear implant coding strategy for tonal language speakers Journal:International Journal of Audiology | 2008 | ||
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 | ||
Pitch and tonal language perception in cochlear implant users Proceeding/Conference:The 2007 Conference on Implantable Auditory Prostheses | 2007 | ||
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 | ||
1989 | |||
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 | ||
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 | ||
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 | ||
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 |