References
- Bigler, E. D., Mortensen, S., Neeley, E. S., Ozonoff, S., Krasny, L., Johnson, M., Lu, J., Provencal, S. L., McMahon, W., & Lainhart, J. E. (2007). Superior temporal gyrus, language function, and autism. Developmental Neuropsychology, 31(2), 217–238. https://doi.org/10.1080/87565640701190841
- Cistaro, A., Quartuccio, N., Piccardo, A., Fania, P., Spunton, M., Liava, A., Danesino, C., Albani, G., & Guala, A. (2020). (18)F-FDG PET identifies altered brain metabolism in patients with cri du chat syndrome. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine, 61(8), 1195–1199. https://doi.org/10.2967/jnumed.119.236893
- Eickhoff, S. B., Heim, S., Zilles, K., & Amunts, K. (2009). A systems perspective on the effective connectivity of overt speech production. Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences, 367(1896), 2399–2421. https://doi.org/10.1098/rsta.2008.0287
- Fang, J. S., Lee, K. F., Huang, C. T., Syu, C. L., Yang, K. J., Wang, L. H., Liao, D. L., & Chen, C. H. (2008). Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion. Clinical Genetics, 73(6), 585–590. https://doi.org/10.1111/j.1399-0004.2008.00995.x
- Fitzgerald, P. H., & Mercer, J. M. (1980). Elimination of an abnormal cell line from blood lymphocytes during post-natal growth. Clinical Genetics, 17(6), 433–436. https://doi.org/https://doi.org/10.1111/j.1399-0004.1980.tb00176.x
- Hogenson, T. (2013). Epigenetics as the underlying mechanism for monozygotic twin discordance. Medical Epigenetics, 1(1), 3–18. https://doi.org/10.1159/000353688
- Iglói, K., Doeller, C. F., Paradis, A. L., Benchenane, K., Berthoz, A., Burgess, N., & Rondi-Reig, L. (2015). Interaction between hippocampus and cerebellum crus i in sequence-based but not place-based navigation. Cerebral Cortex (New York, N.Y. : 1991), 25(11), 4146–4154. https://doi.org/10.1093/cercor/bhu132
- Jonsson, H., Magnusdottir, E., Eggertsson, H. P., Stefansson, O. A., Arnadottir, G. A., Eiriksson, O., Zink, F., Helgason, E. A., Jonsdottir, I., Gylfason, A., Jonasdottir, A., Jonasdottir, A., Beyter, D., Steingrimsdottir, T., Norddahl, G. L., Magnusson, O. T., Masson, G., Halldorsson, B. V., Thorsteinsdottir, U., Helgason, A., … Stefansson, K. (2021). Differences between germline genomes of monozygotic twins. Nature Genetics, 53(1), 27–34. https://doi.org/10.1038/s41588-020-00755-1
- Villa, R., Fergnani, V. G. C., Silipigni, R., Guerneri, S., Cinnante, C., Guala, A., Danesino, C., Scola, E., Conte, G., Fumagalli, M., Gangi, S., Colombo, L., Picciolini, O., Ajmone, P. F., Accogli, A., Madia, F., Tassano, E., Scala, M., Capra, V., Srour, M., … Bedeschi, M. F. (2020). Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations. European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society, 28(1), 110–119. https://doi.org/10.1016/j.ejpn.2020.07.002
- Wolf, U., Rapoport, M. J., & Schweizer, T. A. (2009). Evaluating the affective component of the cerebellar cognitive affective syndrome. The Journal of Neuropsychiatry and Clinical Neurosciences, 21(3), 245–253. https://doi.org/10.1176/appi.neuropsych.21.3.245
- Young, K. D., Erickson, K., Nugent, A. C., Fromm, S. J., Mallinger, A. G., Furey, M. L., & Drevets, W. C. (2012). Functional anatomy of autobiographical memory recall deficits in depression. Psychological Medicine, 42(2), 345–357. https://doi.org/10.1017/s0033291711001371