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

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

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

6. Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients. Issue 3 (19th January 2021)