The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature
Piard, J., Hawkes, L., Milh, M., Villard, L., Borgatti, R., Romaniello, R., Fradin, M., Capri, Y., Héron, D., Nougues, M. -., Nava, C. R., Arsene, O. T., Shears, D., Taylor, J., Pagnamenta, A., Taylor, J. C., Sogawa, Y., Johnson, D., Firth, H., Vasudevan, P., Jones, G., Nguyen-Morel, M. -., Busa, T., Roubertie, A., Van Den Born, M., Brischoux-Boucher, E., Koenig, M., Mignot, C., Kini, U., Philippe, C., Correction to: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3), <<GENETICS IN MEDICINE>>, 2019; 2019 (2019): 1-1+1. [doi:10.1038/s41436-019-0460-y] [http://hdl.handle.net/10807/134378]
Correction to: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3)
Borgatti, Renato;Nava, Consuelo Rubina;
2019
Abstract
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