Browse by Person

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 4.

Article

Martin, H.C., Jones, W.D., McIntyre, R. et al. (37 more authors) (2018) Quantifying the contribution of recessive coding variation to developmental disorders. Science, 362 (6419). pp. 1161-1164. ISSN 0036-8075

Myers, K.A., White, S.M., Mohammed, S. et al. (6 more authors) (2018) Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170]. Epilepsy Research. ISSN 0920-1211

Myers, K.A., White, S.M., Mohammed, S. et al. (6 more authors) (2018) Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome. Epilepsy Research, 140. pp. 166-170. ISSN 0920-1211

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 Mon Oct 21 05:40:22 2019 BST.