The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome

By Kumari Daman   Usdin Karen  

Human Molecular Genetics, Vol. 19, Iss. 23, 2010-12 ,pp. : 4634-4642

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

By  

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

Bentham Science Publishers

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Fibroblast phenotype in male carriers of FMR1 premutation alleles

By Garcia-Arocena Dolores   Yang Jane E.   Brouwer Judith R.   Tassone Flora   Iwahashi Christine   Berry-Kravis Elizabeth M.   Goetz Christopher G.   Sumis Allison M.   Zhou Lili   Nguyen Danh V.   Campos Luis   Howell Erin   Ludwig Anna   Greco Claudia   Willemsen Rob   Hagerman Randi J.   Hagerman Paul J.  

Human Molecular Genetics, Vol. 19, Iss. 2, 2010-01 ,pp. : 299-312

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

Oxford University Press

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Transition from Premutation to Full Mutation in Fragile X Syndrome is Likely to be Prezygotic

By Moutou Céline  

Human Molecular Genetics, Vol. 6, Iss. 7, 1997-07 ,pp. : 971-979

Oxford University Press

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