Barely Significant
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A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene.

Clin Case Rep · 2025 · PMC12313832 · PMID 40756095

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may be significantno p-value reported
However, the relationship between TRPS1 genotype and phenotype is not entirely consistent, and even among carriers of the same gene mutation, there may be significant differences in phenotype.

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