Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach.

Int J Mol Sci · 2023 · PMC10179617 · PMID 37176024

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

may be significantno p-value reported

All these overlapping clinical encumbrances may be significant causes of morbidity and mortality in children with 22q11.2 DS and result in respiratory distress and the need for ventilation support and tracheostomy.

also in 4,300 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.