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

Year Number of Results
2007 3
2010 1
2011 1
2012 1
2013 4
2014 1
2016 3
2017 3
2018 2
2019 5
2020 1
2021 2
2022 2
2023 0
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25 results
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Page 1
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER; Prenatal Assessment of Genomes and Exomes Consortium. Lord J, et al. Among authors: cilliers d. Lancet. 2019 Feb 23;393(10173):747-757. doi: 10.1016/S0140-6736(18)31940-8. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712880 Free PMC article.
The Significance of Squamosal Suture Synostosis.
Eley KA, Thomas GP, Sheerin F, Cilliers D, Wall S, Johnson D. Eley KA, et al. Among authors: cilliers d. J Craniofac Surg. 2016 Sep;27(6):1543-9. doi: 10.1097/SCS.0000000000002888. J Craniofac Surg. 2016. PMID: 27438438
Perrault syndrome: further evidence for genetic heterogeneity.
Jenkinson EM, Clayton-Smith J, Mehta S, Bennett C, Reardon W, Green A, Pearce SH, De Michele G, Conway GS, Cilliers D, Moreton N, Davis JR, Trump D, Newman WG. Jenkinson EM, et al. Among authors: cilliers d. J Neurol. 2012 May;259(5):974-6. doi: 10.1007/s00415-011-6285-5. Epub 2011 Oct 27. J Neurol. 2012. PMID: 22037954 No abstract available.
Cerebro-facio-thoracic dysplasia: expanding the phenotype.
Cilliers D, Alanay Y, Boduroglu K, Utine E, Tunçbilek E, Clayton-Smith J. Cilliers D, et al. Clin Dysmorphol. 2007 Apr;16(2):121-125. doi: 10.1097/MCD.0b013e328012e292. Clin Dysmorphol. 2007. PMID: 17351359
Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
Patterson J, Wellesley D, Morgan S, Cilliers D, Allen S, Gardiner CA; Fetal Genomics Steering Group; UK Clinical Genetics Lead Clinician Group; UK Heads of Genetics Laboratory Group. Patterson J, et al. Among authors: cilliers d. Prenat Diagn. 2021 May;41(6):661-667. doi: 10.1002/pd.5944. Epub 2021 Apr 13. Prenat Diagn. 2021. PMID: 33848363
Diagnostic value of exome and whole genome sequencing in craniosynostosis.
Miller KA, Twigg SR, McGowan SJ, Phipps JM, Fenwick AL, Johnson D, Wall SA, Noons P, Rees KE, Tidey EA, Craft J, Taylor J, Taylor JC, Goos JA, Swagemakers SM, Mathijssen IM, van der Spek PJ, Lord H, Lester T, Abid N, Cilliers D, Hurst JA, Morton JE, Sweeney E, Weber A, Wilson LC, Wilkie AO. Miller KA, et al. Among authors: cilliers d. J Med Genet. 2017 Apr;54(4):260-268. doi: 10.1136/jmedgenet-2016-104215. Epub 2016 Nov 24. J Med Genet. 2017. PMID: 27884935 Free PMC article.
ERF-related craniosynostosis: The phenotypic and developmental profile of a new craniosynostosis syndrome.
Glass GE, O'Hara J, Canham N, Cilliers D, Dunaway D, Fenwick AL, Jeelani NO, Johnson D, Lester T, Lord H, Morton JEV, Nishikawa H, Noons P, Schwiebert K, Shipster C, Taylor-Beadling A, Twigg SRF, Vasudevan P, Wall SA, Wilkie AOM, Wilson LC. Glass GE, et al. Among authors: cilliers d. Am J Med Genet A. 2019 Apr;179(4):615-627. doi: 10.1002/ajmg.a.61073. Epub 2019 Feb 13. Am J Med Genet A. 2019. PMID: 30758909 Free PMC article.
25 results