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Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance.
Genet Med. 2020 Jun;22(6):1005-1014. doi: 10.1038/s41436-020-0766-9. Epub 2020 Mar 3.
Genet Med. 2020.
PMID: 32123317
Free PMC article.
A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project.
Blakes AJM, Wai HA, Davies I, Moledina HE, Ruiz A, Thomas T, Bunyan D, Thomas NS, Burren CP, Greenhalgh L, Lees M, Pichini A, Smithson SF, Taylor Tavares AL, O'Donovan P, Douglas AGL; Genomics England Research Consortium, Splicing and Disease Working Group; Whiffin N, Baralle D, Lord J.
Blakes AJM, et al.
Genome Med. 2022 Jul 26;14(1):79. doi: 10.1186/s13073-022-01087-x.
Genome Med. 2022.
PMID: 35883178
Free PMC article.
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Correction: Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance.
Wai HA, Lord J, Lyon M, Gunning A, Kelly H, Cibin P, Seaby EG, Spiers-Fitzgerald K, Lye J, Ellard S, Thomas NS, Bunyan DJ, Douglas AGL, Baralle D; Splicing and disease working group.
Wai HA, et al.
Genet Med. 2020 Jun;22(6):1129. doi: 10.1038/s41436-020-0789-2.
Genet Med. 2020.
PMID: 32235935
Free PMC article.
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