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Clinica Chimica Acta; International Journal of Clinical Chemistry|September 13, 2005
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndromeChing-Wan Lam, Yuet-Ping Yuen, Wai-Fun Cheng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 5, 2019
Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndromeChing-Wan Lam, Wai-Lan Yeung, Tsz-Ki Ling, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 21, 2010
Circulating fluorocytes at the first attack of acute intermittent porphyria: a missing link in the pathogenesisChing-Wan Lam, Kin-Chong Lau, Chloe Miu Mak, et al.
The American Journal of Chinese Medicine|March 23, 2006
Bilateral frontal activation associated with cutaneous stimulation of elixir field: an FMRI studyAgnes S Chan, Mei-Chun Cheung, Yu Leung Chan, et al.
Epilepsia|August 23, 2006
Effects of illness duration on memory processing of patients with temporal lobe epilepsyMei-chun Cheung, Agnes S Chan, Yu-leung Chan, et al.
American Journal of Medical Genetics. Part A|March 22, 2022
Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literatureHui-Yin Lo, Wai-Fu Ng, Nai-Chung Fong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 2005
DNA-based diagnosis of thyroid hormone resistance syndrome: a novel THRB mutation associated with mild resistance to thyroid hormoneChing-Wan Lam, Angel On-Kei Chan, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 3, 2013
Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiencySun Young Cho, Denise Li-Meng Goh, Kin-Chong Lau, et al.
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