Diagnosis of rare diseases under focus: impacts for Canadian patients.

J Community Genet · 2018 · PMC5752651 · PMID 28733824

Europe PMC DOI

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may be significantno p-value reported

The experiences revealed during the discussions also suggest that the scope of family conflicts and discrimination following the disclosure of a genetic disease may be significant.

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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.