Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings wit...
Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder
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United States: Public Library of Science
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English
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United States: Public Library of Science
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It has been proposed that copy number variations (CNVs) are associated with increased risk of autism spectrum disorder (ASD) and, in conjunction with other genetic changes, contribute to the heterogeneity of ASD phenotypes. Array comparative genomic hybridization (aCGH) and exome sequencing, together with systems genetics and network analyses, are...
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Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder
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TN_cdi_plos_journals_1861455257
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1861455257
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0170386
