Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 2
2019 1
2020 1
2021 1
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

6 results

Results by year

Filters applied: . Clear all
Page 1
Did you mean caron mcanulty (1 results)?
Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia.
Gallon R, Phelps R, Betts L, Hayes C, Masic D, Irving JAE, McAnulty C, Saha V, Vora A, Wimmer K, Motwani J, Macartney C, Burn J, Jackson MS, Moorman AV, Santibanez-Koref M. Gallon R, et al. Among authors: mcanulty c. 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.
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.
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.
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.