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Number of items: 6.

Article

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Blok, LS, Rousseau, J, Twist, J et al. (376 more authors) (2019) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018). Nature Communications, 10. 883. ISSN 2041-1723

Lindley, RI, Anderson, CS, Billot, L et al. (90 more authors) (2017) Family-led rehabilitation after stroke in India (ATTEND): a randomised controlled trial. The Lancet, 390 (10094). pp. 588-599. ISSN 0140-6736

Bengani, H, Handley, M orcid.org/0000-0001-7200-747X, Alvi, M et al. (31 more authors) (2017) Clinical and molecular consequences of disease-associated de novo mutations in SATB2. Genetics in Medicine, 19 (8). pp. 900-908. ISSN 1098-3600

McRae, JF, Clayton, S, Fitzgerald, TW et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542. pp. 433-438. ISSN 0028-0836

Darlington-Pollock, F, Norman, P orcid.org/0000-0002-6211-1625, Lee, AC et al. (3 more authors) (2016) To move or not to move? Exploring the relationship between residential mobility, risk of cardiovascular disease and ethnicity in New Zealand. Social Science & Medicine, 165. pp. 128-140. ISSN 0277-9536

This list was generated on Sun Aug 18 23:03:40 2019 BST.