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The genetic spectrum of CTNNB1-related disease patients
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创建时间：
2022-07-05
相关数据集
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models
The 1.6 Mbp deletion on chromosome 3q29 is associated with a range of neurodevelopmental disorders, including schizophrenia, autism, microcephaly, and intellectual disability. Despite its importance t
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Top eight gene associations with refractive error.
Top eight gene associations with refractive error.
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Additional file 4: Table S3. of Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
Total number of genes of each comorbid condition utilized for this study. Highlighted in blue are ASD sibling disorders. (XLSX 135Â kb)
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Additional file 2 of Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants
Additional file 2: Table S1. Summary of explaining and response variables in the regression analyses. Table S2. Summary of models for relative number of < 1 Mb LOF CNV per gene. Table S3. Mutation
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Additional file 10 of Associative gene networks reveal novel candidates important for ADHD and dyslexia comorbidity
Additional file 10: Table S10. Criteria 9–10 results
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