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Article

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

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

Parry, DA, Holmes, TD, Gamper, N orcid.org/0000-0001-5806-0207 et al. (12 more authors) (2016) A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency. Journal of Allergy and Clinical Immunology, 137 (3). pp. 955-957. ISSN 0091-6749

This list was generated on Sun Oct 13 19:00:22 2019 BST.