Lv2
126 积分 2020-11-05 加入
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss
27天前
已完结
[Guideline for the diagnosis and treatment of Langerhans cell histiocytosis in Chinese children (2026)]
3个月前
已完结
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy
5个月前
已关闭
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy
5个月前
已完结
环状染色体患儿25例的临床表型及遗传学分析
11个月前
已完结
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