Genetic and embryonic transcriptome analyses reveal the molecular and developmental basis of Mayer-Rokitansky-Küster-Hauser syndrome.

J Med Genet · 2026 · PMC12911624 · PMID 41233206

Europe PMC DOI

hedged sentences

0.0100

closest p · 0.2× alpha

0.0100

boldest claim

The sentences

nominally significantp<0.01actually significant

26 Nominally significant genes from the burden test (defined as p<0.01 to minimise noise) were included in the test.

also in 7,732 other papers

did not reach statistical significanceno p-value reported

46 Notably, several previously reported MRKHS candidate genes—such as WNT4, HNF1B and LHX1 —did not reach statistical significance in our mutational burden analysis.

also in 111,027 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.