Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project.

J Med Genet · 2022 · PMC9340050 · PMID 34716235

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likely to be significantno p-value reported

This suggests that there are likely to be significant numbers of participants with ciliopathies recruited to other rare disease categories.

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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.