Lv3
240 积分 2023-08-30 加入
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency
6小时前
待确认
UGT1A1基因c.1091C>T突变与新生儿不明原因高胆红素血症的相关性研究
10小时前
已完结
无虹膜症的临床特点及遗传学研究进展
3个月前
已完结
Research progress on clinical features and genetics of anirida
3个月前
已关闭
人类基因变异的命名规则
3个月前
已完结
Development of phage resistance in multidrug-resistant Klebsiella pneumoniae is associated with reduced virulence: a case report of a personalised phage therapy
9个月前
已完结
Noonan综合征的临床实践指南
11个月前
已完结
中国部分地区新生儿耳聋基因筛查现况调查
1年前
已完结
[Clinical practice guidelines for phenylketonuria]
1年前
已完结
Microbiological and chemical safety of Bombyx mori farmed in north-eastern Italy as a novel food source
1年前
已完结
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