Items where authors include "Clowes, V"

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Number of items: 4.

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

Whitworth, J, Smith, PS, Martin, J-E et al. (330 more authors) (2018) Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes. The American Journal of Human Genetics, 103 (1). pp. 3-18. ISSN 0002-9297

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)

This list was generated on Sat Mar 23 11:44:32 2024 GMT.