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Title | Author(s) | Issue Date | |
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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 | ||
Understanding and perception of direct‐to‐consumer genetic testing in Hong Kong Journal:Journal of Genetic Counseling | 2021 |