Showing results 2 to 5 of 5
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| Title | Author(s) | Issue Date | |
|---|---|---|---|
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 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 | ||
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 |