Dorothy Grange

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2024
Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))
Care4Rare Canada Consortium, Undiagnosed Diseases Network, Mullegama, S. V., Kiernan, K. A., Torti, E., Pavlovsky, E., Tilton, N., Sekula, A., Gao, H., Alaimo, J. T., Engleman, K., Rush, E. T., Blocker, K., Dipple, K. M., Fettig, V. M., Hare, H., Glass, I., Grange, D. K., Griffin, M. & Phornphutkul, C. & 22 others, Massingham, L., Mehta, L., Miller, D. E., Thies, J., Merritt, J. L., Muller, E., Osmond, M., Sawyer, S. L., Slaugh, R., Hickey, R. E., Wolf, B., Choudhary, S., Simonović, M., Zhang, Y., Palculict, T. B., Telegrafi, A., Carere, D. A., Wentzensen, I. M., Morrow, M. M., Monaghan, K. G., Juusola, J. & Yang, J., Jun 6 2024, In: American journal of human genetics. 111, 6, p. 1240 1 p.
Research output: Contribution to journal › Comment/debate

Open Access
2013

Index of suspicion in the nursery: Case 1: Neural Tube Defect in infant of epileptic mother
Moeckel, D., Grange, D. K. & Wambach, J. A., 2013, In: NeoReviews. 14, 8, p. e412-e414
Research output: Contribution to journal › Comment/debate

Research output