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Title:           Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome
Subject:         Human Genomics, 2021, doi:10.1186/s40246-021-00309-4
Keywords:        CNV,Variome,Dystonia,Cerebral palsy,Neuromotor delay,Epilepsy
Author:          Juan L. García-Hernández
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        Title: Background
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       Item: 
        Title: Methods
        Destination: sectionASec2
       Item: 
        Title: Results
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       Item: 
        Title: Conclusions
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     Item: 
      Title: Background
      Destination: sectionSec1
     Item: 
      Title: Materials and methods
      Destination: sectionSec2
      Children: 
       Item: 
        Title: Standard protocol approvals, registrations, and patient consents
        Destination: sectionSec3
       Item: 
        Title: SNP microarray
        Destination: sectionSec4
       Item: 
        Title: Whole exome sequence and comparison with SNP microarray
        Destination: sectionSec5
       Item: 
        Title: Analysis of gene alterations and function associated to clinical phenotypes
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     Item: 
      Title: Results
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       Item: 
        Title: Neuromotor developmental delay phenotype of patient
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       Item: 
        Title: Cooperating CNVs in neuro-pathogenic genes
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      Title: Discussion
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     Item: 
      Title: Conclusion
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     Item: 
      Title: Supplementary Information
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     Item: 
      Title: Abbreviations
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     Item: 
      Title: Authors’ contributions
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     Item: 
      Title: Funding
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     Item: 
      Title: Availability of data and materials
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      Title: Ethics approval and consent to participate
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    Author: Juan L. García-Hernández
    Subject: Human Genomics, 2021, doi:10.1186/s40246-021-00309-4
    Keywords: CNV,Variome,Dystonia,Cerebral palsy,Neuromotor delay,Epilepsy
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