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154. Heteroplasmic mitochondrial DNA variants in cardiovascular diseases

155. Contributors

159. Additional file 1 of Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

162. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency

168. Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study

169. Response to Newman et al.

170. Shortening the diagnostic odyssey-the impact of whole genome sequencing in the NHS

171. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype

172. ANO10 mutations cause ataxia and coenzyme Q10 deficiency

177. Precision mitochondrial medicine.

183. Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)

188. Whole-genome sequencing of patients with rare diseases in a national health system

189. Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1)

190. Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmission

191. Choosing drugs for UK COVID-19 treatment trials

194. Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study

200. Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathy

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