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Showing results (91-100 of 96) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 6, 2026
Magnetically actuated microrobotic system for sequential treatment of biofilmShunyao Li, Yu Mei, Kai Xu, et al.
Journal of Human Genetics|June 24, 2011
Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variantsChloe Miu Mak, Ching-wan Lam, Nai-chung Fong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 23, 2021
Urine organic acid as the first clue towards aromatic L-amino acid decarboxylase (AADC) deficiency in a high prevalence areaTsz-Ki Ling, Ka-Chung Wong, Candace Yim Chan, et al.
Journal of Human Genetics|November 24, 2007
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.
Journal of Human Genetics|February 12, 2020
Erratum to: Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.
Clinical Genetics|February 6, 2020
Clinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong ChineseHan-Chih Hencher Lee, Shun Wong, Bun Sheng, et al.
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Showing results (91-100 of 96) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 96 results.
Proceedings of the National Academy of Sciences of the United States of America|July 6, 2026
Magnetically actuated microrobotic system for sequential treatment of biofilmShunyao Li, Yu Mei, Kai Xu, et al.
Journal of Human Genetics|June 24, 2011
Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variantsChloe Miu Mak, Ching-wan Lam, Nai-chung Fong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 23, 2021
Urine organic acid as the first clue towards aromatic L-amino acid decarboxylase (AADC) deficiency in a high prevalence areaTsz-Ki Ling, Ka-Chung Wong, Candace Yim Chan, et al.
Journal of Human Genetics|November 24, 2007
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.
Journal of Human Genetics|February 12, 2020
Erratum to: Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.
Clinical Genetics|February 6, 2020
Clinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong ChineseHan-Chih Hencher Lee, Shun Wong, Bun Sheng, et al.
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