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Lv4
520 积分
2023-02-08 加入
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Genetic counselors' utilization of ChatGPT in professional practice: A cross‐sectional study
24天前
已完结
Comprehensive Analysis of PKD1 and PKD2 by Long-Read Sequencing in Autosomal Dominant Polycystic Kidney Disease
26天前
已关闭
Molecular genotyping of the Italian cohort of patients with hemophilia B
30天前
已完结
Clinical and Genetic Etiologies of Neonatal Unconjugated Hyperbilirubinemia in the China Neonatal Genomes Project
30天前
已完结
Comprehensive Analysis of PKD1 and PKD2 by Long-Read Sequencing in Autosomal Dominant Polycystic Kidney Disease
1个月前
已关闭
Genotype–phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India
1个月前
已完结
Comprehensive Analysis of PKD1 and PKD2 by Long-Read Sequencing in Autosomal Dominant Polycystic Kidney Disease
1个月前
已关闭
Biological Insights from Cell-Free DNA Methylome Analysis in Preeclampsia
1个月前
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Comparison of Literature Mining Tools for Variant Classification: Through the Lens of Fifty RYR1 Variants
1个月前
已完结
Single gene non‐invasive prenatal screening for autosomal dominant conditions in a high‐risk cohort
1个月前
已完结
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