Lv1
80 积分 2023-09-18 加入
Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0
1天前
已完结
Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients
8天前
已完结
Association of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome
8天前
已完结
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases
10天前
已完结
Optimizing Gene Panels for Equitable Reproductive Carrier Screening: the “Goldilocks” Approach
10天前
已关闭
Comprehensive analysis of thalassemia alleles (CATSA) based on third-generation sequencing is a comprehensive and accurate approach for neonatal thalassemia screening
20天前
已完结
中国异常血红蛋白流行病学的综合分析
28天前
已完结
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome
1个月前
已完结
β-Thalassemias
1个月前
已完结
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