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Rosato S, Unger S, Campos-Xavier B, Caraffi SG, Beltrami L, Pollazzon M, Ivanovski I, Castori M, Bonasoni MP, Comitini G, et al. Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features. Genes. 2022; 13(2):261. https://doi.org/10.3390/genes13020261

Rosato, Simonetta, Sheila Unger, Belinda Campos-Xavier, Stefano Giuseppe Caraffi, Laura Beltrami, Marzia Pollazzon, Ivan Ivanovski, Marco Castori, Maria Paola Bonasoni, Giuseppina Comitini, and et al. 2022. "Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features" Genes 13, no. 2: 261. https://doi.org/10.3390/genes13020261

Rosato, S., Unger, S., Campos-Xavier, B., Caraffi, S. G., Beltrami, L., Pollazzon, M., Ivanovski, I., Castori, M., Bonasoni, M. P., Comitini, G., Nikkels, P. G. J., Lindstrom, K., Umandap, C., Superti-Furga, A., & Garavelli, L. (2022). Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features. Genes, 13(2), 261. https://doi.org/10.3390/genes13020261