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