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50 积分 2024-03-29 加入
Genome Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program
7小时前
待确认
Genome Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program
8小时前
已完结
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
9小时前
已完结
Exploring gene expression signatures in preeclampsia and identifying hub genes through bioinformatic analysis
1个月前
已关闭
MiR-22-3p Suppresses Vascular Remodeling and Oxidative Stress by Targeting CHD9 during the Development of Hypertension
1个月前
已完结
Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions
2个月前
已完结
Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies
5个月前
已完结
Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies
5个月前
已完结
Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies
5个月前
已完结
Cell-Free DNA Screening for Single-Gene Disorders
5个月前
已完结
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