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Mitochondrial Diseases: A Diagnostic Revolution.
Schon KR, Ratnaike T, van den Ameele J, Horvath R, Chinnery PF. Schon KR, et al. Among authors: chinnery pf. Trends Genet. 2020 Sep;36(9):702-717. doi: 10.1016/j.tig.2020.06.009. Epub 2020 Jul 13. Trends Genet. 2020. PMID: 32674947 Review.
Clinical mitochondrial genetics.
Chinnery PF, Howell N, Andrews RM, Turnbull DM. Chinnery PF, et al. J Med Genet. 1999 Jun;36(6):425-36. J Med Genet. 1999. PMID: 10874629 Free PMC article. Review.
Modulating heteroplasmy.
Chinnery PF. Chinnery PF. Trends Genet. 2002 Apr;18(4):173-6. doi: 10.1016/s0168-9525(01)02636-1. Trends Genet. 2002. PMID: 11932010
Searching for nuclear-mitochondrial genes.
Chinnery PF. Chinnery PF. Trends Genet. 2003 Feb;19(2):60-2. doi: 10.1016/s0168-9525(02)00030-6. Trends Genet. 2003. PMID: 12547509 Review.
Risk of developing a mitochondrial DNA deletion disorder.
Chinnery PF, DiMauro S, Shanske S, Schon EA, Zeviani M, Mariotti C, Carrara F, Lombes A, Laforet P, Ogier H, Jaksch M, Lochmüller H, Horvath R, Deschauer M, Thorburn DR, Bindoff LA, Poulton J, Taylor RW, Matthews JN, Turnbull DM. Chinnery PF, et al. Lancet. 2004 Aug 14-20;364(9434):592-6. doi: 10.1016/S0140-6736(04)16851-7. Lancet. 2004. PMID: 15313359
Two direct repeats cause most human mtDNA deletions.
Samuels DC, Schon EA, Chinnery PF. Samuels DC, et al. Among authors: chinnery pf. Trends Genet. 2004 Sep;20(9):393-8. doi: 10.1016/j.tig.2004.07.003. Trends Genet. 2004. PMID: 15313545 Review.
675 results