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Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.
Sci Rep. 2016 Jul 13;6:29506. doi: 10.1038/srep29506.
Sci Rep. 2016.
PMID: 27406733
Free PMC article.
RYR1 mutations are a common cause of congenital myopathies with central nuclei.
Wilmshurst JM, Lillis S, Zhou H, Pillay K, Henderson H, Kress W, Müller CR, Ndondo A, Cloke V, Cullup T, Bertini E, Boennemann C, Straub V, Quinlivan R, Dowling JJ, Al-Sarraj S, Treves S, Abbs S, Manzur AY, Sewry CA, Muntoni F, Jungbluth H.
Wilmshurst JM, et al. Among authors: cloke v.
Ann Neurol. 2010 Nov;68(5):717-26. doi: 10.1002/ana.22119.
Ann Neurol. 2010.
PMID: 20839240
Free article.
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CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting.
Münz M, Ruark E, Renwick A, Ramsay E, Clarke M, Mahamdallie S, Cloke V, Seal S, Strydom A, Lunter G, Rahman N.
Münz M, et al. Among authors: cloke v.
Genome Med. 2015 Jul 28;7(1):76. doi: 10.1186/s13073-015-0195-6.
Genome Med. 2015.
PMID: 26315209
Free PMC article.
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