Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegeneration

By Tan Huiping   Qurashi Abrar   Poidevin Mickael   Nelson David L.   Li He   Jin Peng  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 57-65

Oxford University Press

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Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR

By Crawford Dana C.   Wilson Beth   Sherman StephanieL.  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2909-2918

Oxford University Press

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Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability

By Crawford Dana C.  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1759-1769

Oxford University Press

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Analysis of the Fragile X Trinucleotide Repeat in Basques: Association of Premutation and Intermediate Sizes, Anchoring AGGs and Linked Microsatellites with Unstable Alleles

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Current Genomics, Vol. 9, Iss. 3, 2008-05 ,pp. : 191-199

Bentham Science Publishers

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Haplotype and Interspersion Analysis of the FMR1 CGG Repeat Identifies Two Different Mutational Pathways for the Origin of the Fragile X Syndrome

By Eichler Evan E.   Macpherson James N.   Murray Anna   Jacobs Patricia A.   Chakravarti Aravinda   Nelson David L.  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 319-330

Oxford University Press

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