Items where authors include "Barnicoat, A."

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Article

Edgerley, K., Barnicoat, A., Offiah, A.C. orcid.org/0000-0001-8991-5036 et al. (13 more authors) (2021) AIFM1‐associated X‐linked spondylometaphyseal dysplasia with cerebral hypomyelination. American Journal of Medical Genetics Part A, 185 (4). pp. 1228-1235. ISSN 1552-4825

Yates, T.M., Drucker, M., Barnicoat, A. et al. (19 more authors) (2020) ZMYND11‐related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. Human Mutation, 41 (5). pp. 1042-1050. ISSN 1059-7794

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

This list was generated on Sat Mar 23 06:04:08 2024 GMT.