Somatic Instability of the Myotonic Dystrophy (CTG) n Repeat during Human Fetal Development

By Martorell Loreto  

Human Molecular Genetics, Vol. 6, Iss. 6, 1997-01 ,pp. : 877-880

Oxford University Press

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Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

By Agbulut O.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2717-2726

Oxford University Press

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Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability

By Seznec Hervé   Lia-Baldini Anne-Sophie  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1185-1194

Oxford University Press

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Somatic expansion behaviour of the (CTG) n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch–repair proteins

By te Riele H.   van den Broek W.J.A.A.   Nelen M.R.   Wansink D.G.   Coerwinkel M.M.   Groenen P.J.T.A.   Wieringa B.  

Human Molecular Genetics, Vol. 11, Iss. 2, 2002-01 ,pp. : 191-198

Oxford University Press

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Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients

By Martorell L.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 307-312

Oxford University Press

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