Barely Significant
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Association of RET codon 691 polymorphism in radiation-induced human thyroid tumours with C-cell hyperplasia in peritumoural tissue.

Br J Cancer · 2002 · PMC2375427 · PMID 12085189

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hedged sentence
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highly significantno p-value reported
A highly significant association of RET polymorphisms, specifically the variant A45A, with Hirschsprung disease has also been observed ( Borrego et al , 1999 , 2000 ; Fitze et al , 1999 ).

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