In vitro reactivation of the FMR1 gene involved in fragile X syndrome

By Willemsen R.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 109-113

Oxford University Press

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Premutation and intermediate-size FMR1 alleles in 10 572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

By Morgan K.   Dombrowski C.   Lévesque S.   Morel M.L.   Rouillard P.   Rousseau F.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 371-378

Oxford University Press

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Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio

By Godler David Eugeny   Tassone Flora   Loesch Danuta Zuzanna   Taylor Annette Kimball   Gehling Freya   Hagerman Randi Jenssen   Burgess Trent   Ganesamoorthy Devika   Hennerich Debbie   Gordon Lavinia   Evans Andrew   Choo K.H.   Slater Howard Robert  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1618-1632

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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.  

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Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome

By Tucker Ben   Richards Robert I.   Lardelli Michael  

Human Molecular Genetics, Vol. 15, Iss. 23, 2006-12 ,pp. : 3446-3458

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