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Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation.
Robson SC, Chitty LS, Morris S, Verhoef T, Ambler G, Wellesley DG, Graham R, Leader C, Fisher J, Crolla JA. Robson SC, et al. Among authors: fisher j. Southampton (UK): NIHR Journals Library; 2017 Feb. Southampton (UK): NIHR Journals Library; 2017 Feb. PMID: 28182369 Free Books & Documents. Review.
Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol.
Hill M, Wright D, Daley R, Lewis C, McKay F, Mason S, Lench N, Howarth A, Boustred C, Lo K, Plagnol V, Spencer K, Fisher J, Kroese M, Morris S, Chitty LS. Hill M, et al. Among authors: fisher j. BMC Pregnancy Childbirth. 2014 Jul 16;14:229. doi: 10.1186/1471-2393-14-229. BMC Pregnancy Childbirth. 2014. PMID: 25027965 Free PMC article.
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Chitty LS, Wright D, Hill M, Verhoef TI, Daley R, Lewis C, Mason S, McKay F, Jenkins L, Howarth A, Cameron L, McEwan A, Fisher J, Kroese M, Morris S. Chitty LS, et al. Among authors: fisher j. BMJ. 2016 Jul 4;354:i3426. doi: 10.1136/bmj.i3426. BMJ. 2016. PMID: 27378786 Free PMC article.
"The communication and support from the health professional is incredibly important": A qualitative study exploring the processes and practices that support parental decision-making about postmortem examination.
Lewis C, Riddington M, Hill M, Bevan C, Fisher J, Lyas L, Chalmers A, Arthurs OJ, Hutchinson JC, Chitty LS, Sebire N. Lewis C, et al. Among authors: fisher j. Prenat Diagn. 2019 Dec;39(13):1242-1253. doi: 10.1002/pd.5575. Epub 2019 Nov 4. Prenat Diagn. 2019. PMID: 31682025 Free PMC article.
Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service.
Hill M, Ellard S, Fisher J, Fulop N, Knight M, Kroese M, Ledger J, Leeson-Beevers K, McEwan A, McMullan D, Mellis R, Morris S, Parker M, Tapon D, Baple E, Blackburn L, Choudry A, Lafarge C, McInnes-Dean H, Peter M, Ramakrishnan R, Roberts L, Searle B, Smith E, Walton H, Wynn SL, Han Wu W, Chitty LS. Hill M, et al. Among authors: fisher j. NIHR Open Res. 2022 Jul 18;2:10. doi: 10.3310/nihropenres.13247.2. eCollection 2022. NIHR Open Res. 2022. PMID: 35935673 Free PMC article.
6,241 results