Lv11
40 积分 2025-02-27 加入
The exploration of genetic aetiology and diagnostic strategy for 321 Chinese individuals with intellectual disability
25天前
已完结
Association analysis between chromosomal abnormalities and fetal ultrasonographic soft markers based on 15,263 fetuses
25天前
已完结
Genetic etiology study in a large cohort with congenital insensitivity to pain with anhidrosis
25天前
已完结
Sensitive and visual detection of SARS-CoV-2 using RPA-Cas12a one-step assay with ssDNA-modified crRNA
25天前
已完结
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing
25天前
已完结
X连锁显性遗传性低磷血症性佝偻病诊治专家共识
25天前
已完结
Genebe.net: Implementation and validation of an automatic ACMG variant pathogenicity criteria assignment
1个月前
已完结
Identification of six novel mutations in EDA from 20 hypohidrotic ectodermal dysplasia families
1个月前
已完结
Indexing and searching petabase-scale nucleotide resources
1个月前
已完结
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