Cite

    Castellanos, E., Rosas, I., Negro, A., Gel, B., Alibés, A., Baena, N., Pineda, M., Pi, G., Pintos, G., Salvador, H., Lázaro, C., Blanco, I., Vilageliu, L., Brems, H., Grinberg, D., Legius, E., & Serra, E. (2020). mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical genetics, 97(2), 264–275. http://access.bl.uk/ark:/81055/vdc_100099342854.0x000060