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APA Citation

    Velmans, C., O'Donnell-Luria, A. H., Argilli, E., Tran Mau-them, F., Vitobello, A., Chan, M. C., Fung, J. L., Rech, M., Abicht, A., Aubert Mucca, M., Carmichael, J., Chassaing, N., Clark, R., Coubes, C., Denommé-Pichon, A., de Dios, J. K., England, E., Funalot, B., Gerard, M., Joseph, M., Kennedy, C., Kumps, C., Willems, M., van de Laar, I. M. B., Aarts-Tesselaar, C., van Slegtenhorst, M., Lehalle, D., Leppig, K., Lessmeier, L., Pais, L. S., Paterson, H., Ramanathan, S., Rodan, L. H., Superti-Furga, A., Chung, B. H., Sherr, E., Netzer, C., Schaaf, C. P., & Erger, F. (2022). o'Donnell-Luria-Rodan syndrome: description of a second multinational cohort and refinement of the phenotypic spectrum. Journal of medical genetics, 59(7), 697–705. http://access.bl.uk/ark:/81055/vdc_100158007950.0x000060
  
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