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Search Results to Rosanna Weksberg

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Weksberg, Rosanna

Item TypeName
Concept Autism Spectrum Disorder
Academic Article Structural variation of chromosomes in autism spectrum disorder.
Academic Article Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Academic Article Functional impact of global rare copy number variation in autism spectrum disorders.
Academic Article Autism spectrum disorders and epigenetics.
Academic Article Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder.
Academic Article Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.
Academic Article SHANK1 Deletions in Males with Autism Spectrum Disorder.
Academic Article Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
Academic Article Whole-genome sequencing of quartet families with autism spectrum disorder.
Academic Article Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.
Academic Article Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Academic Article Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Academic Article Epigenetics of Autism Spectrum Disorder.
Academic Article Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.

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  • Autism Spectrum Disorder