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UnknownMapping autism risk loci using genetic linkage and chromosomal rearrangements.
Not available
S-EPMC4867008 | biostudies-literature
UnknownRare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Not available
S-EPMC9653013 | biostudies-literature
UnknownConvergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Not available
S-EPMC4067558 | biostudies-literature
UnknownA genome-wide scan for common alleles affecting risk for autism.
Not available
S-EPMC2947401 | biostudies-literature
UnknownIndividual common variants exert weak effects on the risk for autism spectrum disorders.
Not available
S-EPMC3471395 | biostudies-literature
UnknownA novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Not available
S-EPMC3303079 | biostudies-literature
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