Browsing Centre for Clinical Pharmacology by Author "Rahman, S"
Now showing items 1-4 of 4
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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report
Smedley, D; Smith, KR; Martin, A; Thomas, EA; McDonagh, EM; Cipriani, V; Ellingford, JM; Arno, G; Tucci, A; Vandrovcova, J (2021) -
Author Correction: Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.
Wei, W; Pagnamenta, AT; Gleadall, N; Sanchis-Juan, A; Stephens, J; Broxholme, J; Tuna, S; Odhams, CA; Genomics England Research Consortium; NIHR BioResource (2020-07-22)An amendment to this paper has been published and can be accessed via a link at the top of the paper. -
Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans
Wei, W; Pagnamenta, AT; Gleadall, N; Sanchis-Juan, A; Stephens, J; Broxholme, J; Tuna, S; Odhams, CA; Fratter, C; Turro, E (2020-04-08) -
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study
Schon, KR; Horvath, R; Wei, W; Calabrese, C; Tucci, A; Ibanez, K; Ratnaike, T; Pitceathly, RDS; Bugiardini, E; Quinlivan, R (2021)