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2018 | 2 |
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Page 1
Delivering an accredited non-invasive prenatal diagnosis service for monogenic disorders and recommendations for best practice.
Prenat Diagn. 2018 Jan;38(1):44-51. doi: 10.1002/pd.5197.
Prenat Diagn. 2018.
PMID: 29266293
Review.
Implementation of Multigene Germline and Parallel Somatic Genetic Testing in Epithelial Ovarian Cancer: SIGNPOST Study.
Chandrasekaran D, Sobocan M, Blyuss O, Miller RE, Evans O, Crusz SM, Mills-Baldock T, Sun L, Hammond RFL, Gaba F, Jenkins LA, Ahmed M, Kumar A, Jeyarajah A, Lawrence AC, Brockbank E, Phadnis S, Quigley M, El Khouly F, Wuntakal R, Faruqi A, Trevisan G, Casey L, Burghel GJ, Schlecht H, Bulman M, Smith P, Bowers NL, Legood R, Lockley M, Wallace A, Singh N, Evans DG, Manchanda R.
Chandrasekaran D, et al. Among authors: jenkins la.
Cancers (Basel). 2021 Aug 27;13(17):4344. doi: 10.3390/cancers13174344.
Cancers (Basel). 2021.
PMID: 34503154
Free PMC article.
Item in Clipboard
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton EJ, Legrand A, Benoit V, Roncelin I, Venisse A, Zennaro MC, Jeunemaitre X, Iancu D, Van't Hoff WG, Walsh SB, Godefroid N, Rotthier A, Del Favero J, Devuyst O, Schaefer F, Jenkins LA, Kleta R, Dahan K, Vargas-Poussou R, Bockenhauer D.
Ashton EJ, et al. Among authors: jenkins la.
Kidney Int. 2018 Apr;93(4):961-967. doi: 10.1016/j.kint.2017.10.016. Epub 2018 Feb 15.
Kidney Int. 2018.
PMID: 29398133
Free article.
Item in Clipboard
Patient decision aids in mainstreaming genetic testing for women with ovarian cancer: A prospective cohort study.
Sobocan M, Chandrasekaran D, Sideris M, Blyuss O, Fierheller C, Kalra A, Sia J, Miller RE, Mills-Baldock T, Crusz SM, Sun L, Evans O, Robbani S, Jenkins LA, Ahmed M, Kumar A, Quigley M, Lockley M, Faruqi A, Casey L, Brockbank E, Phadnis S, Trevisan G, Singh N, Legood R, Manchanda R.
Sobocan M, et al. Among authors: jenkins la.
BJOG. 2024 May;131(6):848-857. doi: 10.1111/1471-0528.17675. Epub 2023 Sep 26.
BJOG. 2024.
PMID: 37752678
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Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.
Chitty LS, Mason S, Barrett AN, McKay F, Lench N, Daley R, Jenkins LA.
Chitty LS, et al. Among authors: jenkins la.
Prenat Diagn. 2015 Jul;35(7):656-62. doi: 10.1002/pd.4583. Epub 2015 May 26.
Prenat Diagn. 2015.
PMID: 25728633
Free PMC article.
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