1. 2.3 Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound. (9th June 2014) Authors: Hillman, SC; Carss, K; McMullan, D; Parthiban, V; Maher, E; Kilby, M; Hurles, M Journal: Archives of disease in childhood Issue: Volume 99:Supplement 1(2014) Page Start: A1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Additional information from array comparative genomic hybridisation technology over conventional karyotyping in prenatal diagnosis–a systematic review and meta-analysis. (16th November 2010) Authors: Hillman, SC; Pretlove, S; Coomarasamy, A; McMullan, D; Davison, EV; Maher, E; Kilby, MD Journal: Archives of disease in childhood Issue: Volume 95(2010)Supplement 1 Page Start: Fa4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta‐analysis. (17th July 2013) Authors: Dhillon, RK; Hillman, SC; Morris, RK; McMullan, D; Williams, D; Coomarasamy, A; Kilby, MD Journal: BJOG Issue: Volume 121:Number 1(2014:Jan.) Page Start: 11 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The clinical utility of genetic testing of tissues from pregnancy losses. (5th September 2016) Authors: Waterman, CA; Batstone, P; Bown, N; Cresswell, L; Delmege, C; English, CJ; Fews, G; Grimsley, L; Imrie, S; Kulkarni, A; Mann, K; Johnson, R; Morgan, SM; Roberts, P; Simonic, I; Trueman, S; Wall, M; McMullan, D Journal: BJOG Issue: Volume 125:Number 7(2018) Page Start: 867 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗