Showing results 3 to 9 of 9
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| Title | Author(s) | Issue Date | |
|---|---|---|---|
Exome sequencing in paediatric patients with movement disorders [accepted - OJRD-D-20-00713R2] Journal:Orphanet Journal of Rare Diseases | 2021 | ||
| 2002 | |||
Klein Levin syndrome is a steroid-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis Proceeding/Conference:Hong Kong Medical Journal | 2012 | ||
Myofibrillar myopathies: a clinicopathological study of 13 cases Proceeding/Conference:Asian and Oceanian Myology Center Annual Scentific Meeting, AOMC 2016 | 2016 | ||
Territory wide study of patients with dystrophinopathy in Hong Kong Proceeding/Conference:Neuromuscular Disorders | 2013 | ||
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 | ||
Use of chopsticks in Chinese children Journal:Child: Care, Health and Development | 2002 |