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Yates, T.M., Drucker, M., Barnicoat, A. et al. (19 more authors) (2020) ZMYND11ÔÇÉrelated syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. Human Mutation. ISSN 1059-7794

Yates, T.M., Ng, O.-H., Offiah, A.C. orcid.org/0000-0001-8991-5036 et al. (4 more authors) (2018) Cerebrofaciothoracic dysplasia: four new patients with a recurrent TMCO1 pathogenic variant. American Journal of Medical Genetics Part A. ISSN 1552-4825

Yates, T.M., Suri, M., Desurkar, A. et al. (8 more authors) (2018) SLC35A2-related congenital disorder of glycosylation: Defining the phenotype. European Journal of Paediatric Neurology. ISSN 1090-3798

Yates, T.M., Vasudevan, P.C., Chandler, K.E. et al. (5 more authors) (2017) De novo mutations in HNRNPU result in a neurodevelopmental syndrome. American Journal of Medical Genetics Part A, 173 (11). pp. 3003-3012. ISSN 1552-4825

This list was generated on Sun Jul 5 02:36:52 2020 BST.