Barely Significant
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Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.

Hum Mol Genet · 2022 · PMC8863417 · PMID 34559195

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nominally significantno p-value reported
Indeed, if we include only individuals 15 years or older in analysis, those with Class II deletions were more likely to have a diagnosis of lymphedema, and the p -value becomes nominally significant (0.047).

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