Lv11
44 积分 2022-06-27 加入
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency
1小时前
已完结
Genetic variation in sensation affects food liking and intake
23天前
已完结
Investigating the morphology and genetics of scalp and facial hair characteristics for phenotype prediction
2个月前
已完结
Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA
2个月前
已完结
Genetic variants in PCSK9 in the Japanese population: Rare genetic variants in PCSK9 might collectively contribute to plasma LDL cholesterol levels in the general population
3个月前
已完结
The Lancet Commission to reduce the global burden of sudden cardiac death: a call for multidisciplinary action
6个月前
已完结
Topological Distribution of KCNH2 Variants and Genotype‐Phenotype Relationship in Patients With Long QT Syndrome
6个月前
已完结
Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction
6个月前
已完结
Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing
6个月前
已完结
A contemporary review of sudden cardiac arrest and death in competitive and recreational athletes
6个月前
已完结
皖公网安备34019202002308
