Items where authors include "Male, A"

Article

Vezyroglou, A, Akilapa, R, Barwick, K et al. (26 more authors) (2022) The phenotypic continuum of ATP1A3-related disorders. Neurology, 99 (14). e1511-e1526. ISSN 1526-632X

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

McRae, JF, Clayton, S, Fitzgerald, TW et al. (298 more authors) (2016) Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study. bioRxiv. (Submitted)