Lv41
458 积分 2022-03-04 加入
Nationwide, Couple-Based Genetic Carrier Screening
5小时前
已完结
Nationwide, Couple-Based Genetic Carrier Screening
5小时前
已完结
Meta-analysis of the diagnostic and clinical utility of exome and genome sequencing in pediatric and adult patients with rare diseases across diverse populations
1个月前
已完结
Incremental yield of whole genome sequencing over chromosome microarray and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta‐analysis
1个月前
已完结
Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland
1个月前
已完结
Whole-genome sequencing of patients with rare diseases in a national health system
1个月前
已完结
[Expert consensus on the test development and preliminary implementation of whole genome sequencing for fetal structural abnormalities]
1个月前
已完结
[Consensus on the application of clinical whole genome sequencing in the diagnosis of genetic diseases]
1个月前
已完结
DECoN: A Detection and Visualization Tool for Exonic Copy Number Variants
2个月前
已完结
[Variant analysis for patients from Fujian area with Hong Kong αα type thalassemia]
6个月前
已完结
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