Lv2
178 积分 2025-05-09 加入
染色体微阵列分析在超声异常胎儿产前诊断中的应用价值
4个月前
已完结
Familial imbalance in 16p13.11 leads to a dosage compensation rearrangement in an unaffected carrier
4个月前
已完结
Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks
4个月前
已完结
Utilizing ClinGen gene‐disease validity and dosage sensitivity curations to inform variant classification
4个月前
已完结
The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis
4个月前
已完结
Prenatal genomic sequencing: Navigating uncertainty
4个月前
已完结
Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
7个月前
已关闭
A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment
7个月前
已完结
The Challenge of Genetic Variants of Uncertain Clinical Significance
8个月前
已完结
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