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UnknownThe Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
Not available
S-EPMC5798982 | biostudies-literature
UnknownComplex genomic rearrangements in the dystrophin gene due to replication-based mechanisms.
Not available
S-EPMC4303224 | biostudies-literature
UnknownImpact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Not available
S-EPMC5708103 | biostudies-literature
UnknownClinically relevant copy number variations detected in cerebral palsy.
Not available
S-EPMC4532872 | biostudies-literature
UnknownGenome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity.
Not available
S-EPMC7509619 | biostudies-literature
UnknownGene copy number variation and pediatric mental health/neurodevelopment in a general population.
Not available
S-EPMC10360394 | biostudies-literature
UnknownGenome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.
Not available
S-EPMC9617891 | biostudies-literature
UnknownRCL1 copy number variants are associated with a range of neuropsychiatric phenotypes.
Not available
S-EPMC8159744 | biostudies-literature
UnknownCopy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.
Not available
S-EPMC7374944 | biostudies-literature
UnknownObservation of quantum entanglement with top quarks at the ATLAS detector.
Not available
S-EPMC11410654 | biostudies-literature
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