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Year | Number of Results |
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2019 | 2 |
2022 | 1 |
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2024 | 1 |
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Page 1
Systematic review of differential methylation in rare ophthalmic diseases.
BMJ Open Ophthalmol. 2019 Nov 13;4(1):e000342. doi: 10.1136/bmjophth-2019-000342. eCollection 2019.
BMJ Open Ophthalmol. 2019.
PMID: 31799411
Free PMC article.
Review.
A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland.
Kerr K, McKenna C, Heggarty S, Bailie C, McMullan J, Crowe A, Kilner J, Donnelly M, Boyle S, Rea G, Flanagan C, McKee S, McKnight AJ.
Kerr K, et al. Among authors: flanagan c.
Genes (Basel). 2022 Jun 21;13(7):1104. doi: 10.3390/genes13071104.
Genes (Basel). 2022.
PMID: 35885887
Free PMC article.
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Differential methylation as a diagnostic biomarker of rare renal diseases: a systematic review.
Kerr K, McAneney H, Flanagan C, Maxwell AP, McKnight AJ.
Kerr K, et al. Among authors: flanagan c.
BMC Nephrol. 2019 Aug 16;20(1):320. doi: 10.1186/s12882-019-1517-5.
BMC Nephrol. 2019.
PMID: 31419951
Free PMC article.
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When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta-analysis.
Sonner S, Reilly K, Woolf AS, Chandler N, Kilby MD, Maher ER, Flanagan C, McKnight AJ, Mone F.
Sonner S, et al. Among authors: flanagan c.
Prenat Diagn. 2024 Feb;44(2):187-195. doi: 10.1002/pd.6479. Epub 2023 Dec 6.
Prenat Diagn. 2024.
PMID: 38056891
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