Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion.

Prenat Diagn · 2017 · PMC5525582 · PMID 28497584

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

likely to be significantno p-value reported

As such, there is likely to be significant variation in reporting some aspects of this testing, for example reporting fetal gender, screening for sex chromosome aneuploidies and other chromosome rearrangements.

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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.