Lv1
40 积分 2021-05-25 加入
Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis
5个月前
已完结
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
1年前
已完结
Whole exome sequencing and transcriptome analysis in two unrelated patients with novel SET mutations
1年前
已完结
An atlas of genetic scores to predict multi-omic traits
1年前
已完结
High-Resolution and Noninvasive Fetal Exome Screening
1年前
已完结
High-Resolution and Noninvasive Fetal Exome Screening
1年前
已关闭
Detection of aberrant gene expression events in RNA sequencing data
1年前
已完结
Integrative analysis reveals the recurrent genetic etiologies in idiopathic pulmonary fibrosis
1年前
已完结
Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression
1年前
已完结
Genome sequencing detects a wide range of clinically relevant copy number variants and other genomic alterations
1年前
已关闭
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