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UnknownBiallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies.
Not available
S-EPMC9090724 | biostudies-literature
UnknownGenome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Not available
S-EPMC1665641 | biostudies-literature
UnknownThe Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
Not available
S-EPMC5798982 | biostudies-literature
UnknownAn inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
Not available
S-EPMC2649013 | biostudies-literature
UnknownChromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomics.
Not available
S-EPMC9339297 | biostudies-literature
UnknownInherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology.
Not available
S-EPMC3276277 | biostudies-literature
UnknownGenome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.
Not available
S-EPMC6559655 | biostudies-literature
Genomicsena-DATASET-TCAG_HSC-21-02-2017-04:02:43:010-730 - samples
TBD
EGAD00001003187 | EGA
UnknownComparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5.
Not available
S-EPMC29746 | biostudies-literature
UnknownAutism spectrum disorder: advances in evidence-based practice.
Not available
S-EPMC3986314 | biostudies-literature
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