Lv1
48 积分 2025-03-11 加入
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
1个月前
已完结
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data
1个月前
已完结
The utility of exome sequencing in diagnosing pediatric neurodevelopmental disorders in a highly consanguineous population
1个月前
已完结
Splicing in action: assessing disease causing sequence changes
1个月前
已完结
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
1个月前
已完结
De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations
2个月前
已完结
Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome
2个月前
已完结
Cognitive Outcomes of Extremely Preterm Infants at 6.5 Years after Postnatal Corticosteroid Treatment: A Pilot Study
2个月前
已完结
Prenatal glucocorticoids exposure disrupts maturation of a cluster of microglia, causing poor social memory and more repetitive behaviors
3个月前
已完结
ROP-GAN: an image synthesis method for retinopathy of prematurity based on generative adversarial network
4个月前
已完结
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