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勤奋的雅霜
Lv1
20 积分
2023-02-06 加入
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Autosomal Dominant Polycystic Kidney Disease
15天前
已完结
Structure of the human PKD1-PKD2 complex
16天前
已完结
Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients
20天前
已完结
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay
1个月前
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De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay
1个月前
已完结
Whole exome sequencing approach for identification of the molecular etiology in pediatric patients with hematuria
3个月前
已完结
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies
3个月前
已完结
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
3个月前
已完结
DNA methylation episignature, extension of the clinical features and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7
4个月前
已完结
Genetic Association of Lipids and Lipid-Lowering Drug Target Genes With Attention Deficit Hyperactivity Disorder
4个月前
已完结
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