Author:
Cianfaglione Rina,Meek Andrea,Clarke Angus,Kerr Michael,Hastings Richard P.,Felce David
Funder
NISCHR Social Care Studentship scheme
Publisher
Springer Science and Business Media LLC
Subject
Developmental and Educational Psychology,Physical Therapy, Sports Therapy and Rehabilitation
Reference28 articles.
1. Amir, R. E., Veyver, I. B., Wan, M., Tran, C. Q., Franckle, U., & Zoghbi, H. Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG – binding protein 2. Nature Genetics, 23, 185–187.
2. Cass, H., Reilly, S., Owen, L., Wisbeach, A., Weekes, L., Slonims, V., et al. (2003). Findings from a multidisciplinary clinical case series of females with rett syndrome. Developmental Medicine and Child Neurology, 45, 325–337.
3. Cianfaglione, R., Clarke, A., Kerr, M., Hastings, R. P., Oliver, C., Moss, J., et al. (2015a). A national survey of rett syndrome: behavioural characteristics. Journal of Neurodevelopmental Disorders, 7, 11.
4. Cianfaglione, R., Clarke, A., Kerr, M., Hastings, R. P., Oliver, C., & Felce, D. (2015b). A national survey of Rett syndrome: Age, clinical characteristics, current abilities and health. American Journal of Medical Genetics Part A, 167a, 1493–1500.
5. Coleman, M., Brubaker, J., Hunter, K., & Smith, G. (1988). Rett syndrome: A survey of North American patients. Journal of Mental Deficiency Research, 32, 117–124.
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献