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The columns represent patients and their relatives. The cytogenetic and molecular findings are placed and ordered on the raws.
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2018-12-05
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Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetrance
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Additional file 2 of Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes
Additional file 2: Table S1. Subject characteristics in relation to outcome at 36 months. Table S2. Subject characteristics table by subject. Table S3. Associations between ASD diagnosis, global CpG m
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Genotyping of the six novel rare missense variations in the follow-up study.
ASD, autism spectrum disorder; CI, confidence interval; MAF, mutant allele frequency; OR, odds ratio.aGenotypes: reference and mutant alleles are denoted by 1 and 2, respectively.Genotyping of the six
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