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UnknownGenome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.
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S-EPMC4320806 | biostudies-literature
UnknownVariants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.
Not available
S-EPMC8206167 | biostudies-literature
UnknownSNAPSHOT USA 2020: A second coordinated national camera trap survey of the United States during the COVID-19 pandemic.
Not available
S-EPMC9347782 | biostudies-literature
UnknownCHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476 | biostudies-literature
UnknownMutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects.
Not available
S-EPMC5392243 | biostudies-literature
UnknownFinding Diagnostically Useful Patterns in Quantitative Phenotypic Data.
Not available
S-EPMC6848993 | biostudies-literature
UnknownLarge-scale discovery of novel genetic causes of developmental disorders.
Not available
S-EPMC5955210 | biostudies-literature
UnknownPrevalence and architecture of de novo mutations in developmental disorders.
Not available
S-EPMC6016744 | biostudies-literature
UnknownGenetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Not available
S-EPMC4392068 | biostudies-literature
UnknownHistone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.
Not available
S-EPMC5778085 | biostudies-literature
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