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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Analysis of Germline Variation at the FMR1 CGG Repeat Shows Variation in the Normal-Premutated Borderline Range

By Monet Etienne   Chateau Corinne   Hirst Mark C.   Thepot François   Taillandier Agnès   Cibois Olivier   Serre Jean-Louis  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 821-825

Oxford University Press

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A fragile balance: FMR1 expression levels

By Oostra Ben A.   Willemsen Rob  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 249-257

Oxford University Press

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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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Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

By Hennah William  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3151-3159

Oxford University Press

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