Author:
Reyniers Edwin,Vits Lieve,De Boulle Kristel,Roy Bernadette Van,Velzen Desirée Van,de Graaff Esther,Verkerk Annemieke J.M.H.,Jorens Hugo Z.J.,Darby John K.,Oostra Ben,Willems Patrick J.
Publisher
Springer Science and Business Media LLC
Reference44 articles.
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2. Gedeon, A.K. et al. Fragile X syndrome without CGG amplification has an FMR–1 deletion. Nature Genet. 1, 341–344 (1992).
3. Wöhrle, D. et al. A microdeletion of less than 250 kb, including the proximal part of the FMR–1 gene and the fragile site, in a male with the clinical phenotype of the fragile X syndrome. Am. J. hum. Genet. 51, 299–306 (1992).
4. De Boulle, K. et al. A point mutation in the FMR–1 gene associated with fragile X mental retardation. Nature Genet. 3, 31–35 (1993).
5. Kremer, E. et al. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CGG)n . Science 252, 1711–1714 (1991).
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