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UnknownA CLASP-modulated cell edge barrier mechanism drives cell-wide cortical microtubule organization in Arabidopsis.
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S-EPMC3265373 | biostudies-literature
UnknownAnatomy of DNA methylation signatures: Emerging insights and applications.
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S-EPMC8387466 | biostudies-literature
UnknownPsychopharmacology in children with genetic disorders of epigenetic and chromatin regulation.
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S-EPMC12023381 | biostudies-literature
UnknownTransition services in 22q11 deletion syndrome: Hit or miss.
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S-EPMC12481110 | biostudies-literature
UnknownANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome.
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S-EPMC10117159 | biostudies-literature
UnknownThe utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorder.
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S-EPMC9303780 | biostudies-literature
UnknownGenome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
Not available
S-EPMC6189095 | biostudies-literature
UnknownExpanding the neurodevelopmental phenotypes of individuals with de novo <i>KMT2A</i> variants.
Not available
S-EPMC6486600 | biostudies-literature
UnknownFunctional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
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S-EPMC6636171 | biostudies-literature
UnknownPractical guidelines for managing adults with 22q11.2 deletion syndrome.
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S-EPMC4526275 | biostudies-literature
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