Modeling fragile X syndrome in the Fmr1 knockout mouse
Author:
Affiliation:
1. MIND Institute, Department of Psychiatry and Behavioral Sciences, University of California, Davis, School of Medicine
Publisher
International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)
Subject
General Medicine
Reference211 articles.
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2. 2. Rogers SJ, Wehner DE, Hagerman R. The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr. 2001; 22:409-417.
3. 3. Turner G, Webb T, Wake S, Robinson H. Prevalence of fragile X syndrome. American journal of medical genetics. Am J Med Genet. 1996; 64:196-197.
4. 4. Murray A, Youings S, Dennis N, Latsky L, Linehan P, McKechnie N, Macpherson J, Pound M, Jacobs P. Population screening at the FRAXA and FRAXE loci: Molecular analyses of boys with learning difficulties and their mothers. Hum Mol Genet. 1996; 5:727-735.
5. 5. Pembrey ME, Barnicoat AJ, Carmichael B, Bobrow M, Turner G. An assessment of screening strategies for fragile X syndrome in the UK. Health Technol Assess. 2001; 5:1-95.
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