Romanelli, V., Belinchón, A., Benito‐Sanz, S., Martínez‐Glez, V., Gracia‐Bouthelier, R., Heath, K. E., Campos‐Barros, A., García‐Miñaur, S., Fernandez, L., Meneses, H., López‐Siguero, J. P., Guillén‐Navarro, E., Gómez‐Puertas, P., Wesselink, J., Mercado, G., Esteban‐Marfil, V., Palomo, R., Mena, R., Sánchez, A., … Lapunzina, P. (2010). CDKN1C (p57Kip2) analysis in Beckwith–Wiedemann syndrome (BWS) patients: Genotype–phenotype correlations, novel mutations, and polymorphisms. American Journal of Medical Genetics Part A, 152A(6), 1390–1397. Portico. https://doi.org/10.1002/ajmg.a.33453
