Barely Significant
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Advances in understanding - genetic basis of intellectual disability.

F1000Res · 2016 · PMC4830215 · PMID 27127621

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highly significantno p-value reported
Interestingly, when the Human Phenotype Ontology terms are examined (see Supplementary Table 4e ), the first two terms of the list (with a highly significant p value of 9.61 × 10 -297 ) are “Neurodevelopmental abnormality” and “Intellectual disability”, followed by “Abnormality of nervous system physiology” ( p value: 7.36 × 10 -169 ) and “Neurodevelopmental delay” ( p value: 9.14 × 10 -143 ).

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