The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay. Wayhelova Marketa et al. BMC medical genomics 2019 12(1) 111

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Last Posted: Jan 10, 2020

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• The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
  Wayhelova Marketa et al. BMC medical genomics 2019 12(1) 111
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• Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes.
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• Why parents consent to their children's participation in genetic research: A study of parental decision making.
  Kumari Sunita et al. Indian journal of medical ethics 4 (NS)(4)
• Artificial intelligence for precision medicine in neurodevelopmental disorders.
  Uddin Mohammed et al. NPJ digital medicine 2019 2112
• Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
  D'Abate L et al. Nature communications 2019 Dec (1) 5519

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