Items where authors include "Chandler, K.E."

Article

Aughey, G.N., Cali, E., Maroofian, R. orcid.org/0000-0001-6763-1542 et al. (53 more authors) (2024) Clinical and genetic characterization of a progressive RBL2 associated neurodevelopmental disorder. Brain. ISSN 0006-8950

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

Keppler-Noreuil, K.M., Sapp, J.C., Lindhurst, M.J. et al. (28 more authors) (2014) Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. Am J Med Genet A, 164A (7). pp. 1713-1733. ISSN 1552-4825