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Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
12小时前
已完结
Variant frequency of GJB2 c.109G>A (p.Val37Ile) in the general Chinese population: A systematic review and meta-analysis
3天前
已完结
Hirschsprung disease
9天前
已完结
SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism
9天前
已完结
The effects of microbiota-derived short-chain fatty acids on T lymphocytes: From autoimmune diseases to cancer
2个月前
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