Fragile X syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg200861.pdf
Reference50 articles.
1. Crawford DC, Acuna JM, Sherman SL : FMR1 and the fragile X syndrome: human genome epidemiology review. Genet Med 2001; 3: 359–371.
2. Sherman SL, Jacobs PA, Morton NE et al: Further segregation analysis of the fragile X syndrome with special reference to transmitting males. Hum Genet 1985; 69: 289–299.
3. Maes B, Fryns JP, Ghesquiere P, Borghgraef M : Phenotypic checklist to screen for fragile X syndrome in people with mental retardation. Ment Retard 2000; 38: 207–215.
4. Merenstein SA, Sobesky WE, Taylor AK, Riddle JE, Tran HX, Hagerman RJ : Molecular-clinical correlations in males with an expanded FMR1 mutation. Am J Med Genet 1996; 64: 388–394.
5. Kemper MB, Hagerman RJ, Altshul-Stark D : Cognitive profiles of boys with the fragile X syndrome. Am J Med Genet 1988; 30: 191–200.
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