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You searched for: Author/Creator Fan, Yanbin

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1. Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients. Issue 5 (22nd June 2020)

2. Congenital muscular dystrophies in China. Issue 3 (6th June 2019)

4. Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy. Issue 1 (December 2018)

7. GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome. Issue 2 (18th June 2020)