Duplication 7 Syndrome
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-56782-2_9140-2
Reference43 articles.
1. Belmonte, M. K., & Bourgeron, T. (2006). Fragile X syndrome and autism at the intersection of genetic and neural networks. Nature Neuroscience, 9(10), 1221–1225. nn1765 [pii].
2. Berg, J. S., Brunetti-Pierri, N., Peters, S. U., Kang, S. H., Fong, C. T., Salamone, J., …, Cheung, S. W. (2007). Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region. Genetics in Medicine, 9(7), 427–441. https://doi.org/10.1097/GIM.0b013e3180986192 .
3. Berg, J. S., Potocki, L., & Bacino, C. A. (2010). Common recurrent microduplication syndromes: Diagnosis and management in clinical practice. American Journal of Medical Genetics. Part A, 152A(5), 1066–1078. https://doi.org/10.1002/ajmg.a.33185 .
4. Betancur, C. (2011). Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting. Brain Research, 1380, 42–77. https://doi.org/10.1016/j.brainres.2010.11.078 .
5. Beunders, G., van de Kamp, J. M., Veenhoven, R. H., van Hagen, J. M., Nieuwint, A. W., & Sistermans, E. A. (2010). A triplication of the Williams-Beuren syndrome region in a patient with mental retardation, a severe expressive language delay, behavioural problems and dysmorphisms. Journal of Medical Genetics, 47(4), 271–275. https://doi.org/10.1136/jmg.2009.070490 .
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