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Hencher H.C. Lee
Hencher H.C. Lee
Medicine
Pathology
Multiplex ligation-dependent probe amplification
Citrin deficiency
Immunology
3
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3
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0
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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.
2020
Molecular Genetics & Genomic Medicine
K.S. Yeung
Florrie N. Y. Yu
Cheuk Wing Fung
Sheila Wong
Hencher H.C. Lee
Sharon Tsui-hang Fung
Genevieve P.G. Fung
K. Y. Leung
Wai Hang Chung
Yun-Ting Lee
Vivian K. S. Ng
Mullin H.C. Yu
Jasmine L.F. Fung
Mandy H.Y. Tsang
Kelvin Y. K. Chan
Sophelia H.S. Chan
Anita S. Y. Kan
Brian H.Y. Chung
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Detection of gross deletions in SLC25A13 with in-house multiplex ligation-dependent probe amplification (MLPA) probemix for molecular diagnosis of citrin deficiency
2019
Pathology
Nike K.C. Lau
Hencher H.C. Lee
Sammy Pak-Lam Chen
Ck Ching
Chi Chung Shek
Yuet-Ping Yuen
Chloe Miu Mak
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Slimming agent related toxicity – a 10-year review at a tertiary toxicology laboratory in Hong Kong
2019
Pathology
Nike K.C. Lau
Yk Chong
Ck Ching
Sammy Pak-Lam Chen
Hencher H.C. Lee
Tony Wl Mak
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