1. Aminoglycoside-induced deafness during treatment of acute leukaemia. Issue 2 (19th February 2010) Authors: Bitner-Glindzicz, M; Osei-Lah, V; Colvin, I; Sirimanna, T; Lucas, D; Ardle, B Mac; Webb, D; Shankar, A; Kingston, J; Jenkins, L; Rahman, S Journal: Archives of disease in childhood Issue: Volume 95:Issue 2(2010) Page Start: 153 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. B2.1 100, 000 genomes project at gosh: experience from 111 pilot families. (4th October 2017) Authors: Clement, E; Buckton, A; Ashton, E; Scott, R; Beales, P; Loughlin, S; Bitner-Glindzicz, M; Jenkins, L Journal: Archives of disease in childhood Issue: Volume 102(2017)Supplement 3 Page Start: A9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. B2.4 Rapid paediatric sequencing (raps) in critically ill children at great ormond street hospital. (4th October 2017) Authors: Clement, E; Boukhibar, L; Jones, W; Hurst, J; Scott, R; Chitty, L; Bitner-Glindzicz, M; Peters, M; Williams, H; Beales, P Journal: Archives of disease in childhood Issue: Volume 102(2017)Supplement 3 Page Start: A10 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families. Issue 12 (December 1994) Authors: Bitner-Glindzicz, M; de Kok, Y; Summers, D; Huber, I; Cremers, F P; Ropers, H H; Reardon, W; Pembrey, M E; Malcolm, S Journal: Journal of medical genetics Issue: Volume 31:Issue 12(1994) Page Start: 916 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. P449The novel long QT syndrome type 1 mutation KCNQ1-p.Thr247dup causes severe channel dysfunction but retains preserved adrenergic regulation. (19th March 2018) Authors: Rathod, V S; Harmer, S C; Salsbury, G A; Bitner-Glindzicz, M; Lambiase, P D; Tinker, A Journal: Europace Issue: Volume 20(2018)Supplement 1 Page Start: i87 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment. Issue 4 (1st April 2001) Authors: Hutchin, T P; Thompson, K R; Parker, M; Newton, V; Bitner-Glindzicz, M; Mueller, R F Journal: Journal of medical genetics Issue: Volume 38:Issue 4(2001) Page Start: 229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗