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caron mcanulty
(1 results)?
Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia.
Leuk Lymphoma. 2023 Jan;64(1):217-220. doi: 10.1080/10428194.2022.2131412. Epub 2022 Oct 22.
Leuk Lymphoma. 2023.
PMID: 36272172
No abstract available.
Sequencing-based microsatellite instability testing using as few as six markers for high-throughput clinical diagnostics.
Gallon R, Sheth H, Hayes C, Redford L, Alhilal G, O'Brien O, Spiewak H, Waltham A, McAnulty C, Izuogu OG, Arends MJ, Oniscu A, Alonso AM, Laguna SM, Borthwick GM, Santibanez-Koref M, Jackson MS, Burn J.
Gallon R, et al. Among authors: mcanulty c.
Hum Mutat. 2020 Jan;41(1):332-341. doi: 10.1002/humu.23906. Epub 2019 Sep 15.
Hum Mutat. 2020.
PMID: 31471937
Free PMC article.
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Detection of Microsatellite Instability in Colonoscopic Biopsies and Postal Urine Samples from Lynch Syndrome Cancer Patients Using a Multiplex PCR Assay.
Phelps R, Gallon R, Hayes C, Glover E, Gibson P, Edidi I, Lee T, Mills S, Shaw A, Heer R, Ralte A, McAnulty C, Santibanez-Koref M, Burn J, Jackson MS.
Phelps R, et al. Among authors: mcanulty c.
Cancers (Basel). 2022 Aug 8;14(15):3838. doi: 10.3390/cancers14153838.
Cancers (Basel). 2022.
PMID: 35954501
Free PMC article.
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Improving the identification of patients with a genetic diagnosis of familial hypercholesterolaemia in primary care: A strategy to achieve the NHS long term plan.
Ingoe L, Potter A, Musson S, Neely D, Pilkington G, Allen AJ, Reay D, Luvai A, McAnulty C, Camm N, Berry I, Nichols J, Forbes G, Newton J, Carey PE.
Ingoe L, et al. Among authors: mcanulty c.
Atherosclerosis. 2021 May;325:38-45. doi: 10.1016/j.atherosclerosis.2021.03.035. Epub 2021 Apr 2.
Atherosclerosis. 2021.
PMID: 33892327
Free article.
Item in Clipboard
Utility of genetic testing in suspected familial cranial diabetes insipidus.
Srinivasan R, Ball S, Ward-Platt M, Bourn D, McAnulty C, Cheetham T.
Srinivasan R, et al. Among authors: mcanulty c.
Endocrinol Diabetes Metab Case Rep. 2013;2013:130068. doi: 10.1530/EDM-13-0068. Epub 2013 Oct 21.
Endocrinol Diabetes Metab Case Rep. 2013.
PMID: 24616780
Free PMC article.
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Juvenile idiopathic arthritis, mitral valve prolapse and a familial variant involving the integrin-binding fragment of FBN1.
Wilson BT, Jensen SA, McAnulty CP, Brennan P, Handford PA.
Wilson BT, et al. Among authors: mcanulty cp.
Am J Med Genet A. 2013 Aug;161A(8):2047-51. doi: 10.1002/ajmg.a.36011. Epub 2013 Jun 21.
Am J Med Genet A. 2013.
PMID: 23794388
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