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138 积分 2022-08-24 加入
Expanded carrier screening in China: a focused narrative review and conceptual implementation framework
1天前
已完结
Long-read sequencing resolves complex CYP21A2 variants and identifies 2+0 carriers in 21-hydroxylase deficiency
23天前
已完结
Novel compound heterozygous SIL1 variants associated with Marinesco-Sjögren syndrome in a Chinese family
1个月前
已完结
Genetic landscape of hereditary cardiomyopathies and arrhythmias in China
1个月前
已完结
Effects of breviscapine and C3435T MDR1 gene polymorphism on the pharmacokinetics of fexofenadine, a P-glycoprotein substrate, in healthy volunteers
1个月前
已完结
漳州地区8 182例育龄人群脊髓性肌萎缩症携带者筛查及产前诊断结果的分析
1个月前
已完结
Gene-gene interactions and associations of six hypertension related single nucleotide polymorphisms with obesity risk in a Chinese children population
2个月前
已完结
The first genome-wide association study on pediatric obesity in Taiwan
2个月前
已完结
伐地那非治疗 II 型糖尿病患者勃起功能障碍的临床观察
1年前
已采纳
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