1. A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly. Issue 4 (11th February 2018) Authors: Ishida, M.; Cullup, T.; Boustred, C.; James, C.; Docker, J.; English, C.; Lench, N.; Copp, A.J.; Moore, G.E.; Greene, N.D.E.; Stanier, P. Journal: Clinical genetics Issue: Volume 93:Issue 4(2018) Page Start: 870 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family. (June 2019) Authors: Seselgyte, R.; Bryant, D.; Demetriou, C.; Ishida, M.; Peskett, E.; Moreno, N.; Morrogh, D.; Sell, D.; Lees, M.; Farrall, M.; Moore, G.E.; Sommerlad, B.; Pauws, E.; Stanier, P. Journal: Journal of dental research Issue: Volume 98:Number 6(2019) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss‐of‐function vs missense variants. Issue 5 (26th July 2016) Authors: Savastano, C.P.; Brito, L.A.; Faria, Á.C.; Setó‐Salvia, N.; Peskett, E.; Musso, C.M.; Alvizi, L.; Ezquina, S.A.M.; James, C.; GOSgene, ; Beales, P.; Lees, M.; Moore, G.E.; Stanier, P.; Passos‐Bueno, M.R. Journal: Clinical genetics Issue: Volume 91:Issue 5(2017) Page Start: 683 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors. Issue 6704 (7th October 1989) Authors: Stanier, P.; Taylor, D. L.; Kitchen, A. D.; Wales, N.; Tryhorn, Y.; Tyms, A. S. Journal: BMJ Issue: Volume 299:Issue 6704(1989) Page Start: 897 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗