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Polygenic Risk Scores and Hearing Loss Phenotypes in Children
4天前
已完结
SF3B4 Frameshift Variants Represented a More Severe Clinical Manifestation in Nager Syndrome
9天前
已完结
Rare germline structural variants increase risk for pediatric solid tumors
20天前
已完结
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years
22天前
已完结
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing
22天前
已完结
Gene and phenome-based analysis of the shared genetic architecture of eye diseases
1个月前
已完结
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection
1个月前
已完结
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial
1个月前
已完结
Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions
1个月前
已完结
Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years
1个月前
已关闭
A Janus dual-atom catalyst for electrocatalytic oxygen reduction and evolution
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