Instability of a (CGG) 98 repeat in the Fmr1 promoter

By Hirst M.C.   Bontekoe C.J.M.   Bakker C.E.   Nieuwenhuizen I.M.   van der Linde H.   Lans H.   de Lange D.   Oostra B.A.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1693-1699

Oxford University Press

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Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development

By Cunningham Christopher L.   Martnez Cerdeo Vernica   Navarro Porras Eliecer   Prakash Anish N.   Angelastro James M.   Willemsen Rob   Hagerman Paul J.   Pessah Isaac N.   Berman Robert F.   Noctor Stephen C.  

Human Molecular Genetics, Vol. 20, Iss. 1, 2011-01 ,pp. : 64-79

Oxford University Press

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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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Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance

By Allen Emily  

Behavior Genetics, Vol. 35, Iss. 4, 2005-07 ,pp. : 435-445

Springer Publishing Company

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The (CGG) n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter

By Chen Li-Sheng   Tassone Flora   Sahota Parminder   Hagerman Paul J.  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3067-3074

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