Publications by authors named "Merran Finnis"

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Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).
Tod Fullston, Louise Brueton, Tracey Willis, Sunny Philip, Lesley MacPherson, Merran Finnis

Eur J Hum Genet· February 2010

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Common chromosomal fragile site FRA16D mutation in cancer cells.
Merran Finnis, Sonia Dayan, Lynne Hobson, Georgia Chenevix-Trench, Kathryn Friend

Hum Mol Genet· May 2005

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XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene.
Monica L Stepp, A Lauren Cason, Merran Finnis, Marie Mangelsdorf, Elke Holinski-Feder

BMC Med Genet· April 2005

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Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
Theologia Sarafidou, Christina Kahl, Isabel Martinez-Garay, Marie Mangelsdorf, Stefan Gesk, Merran Finnis

Genomics· July 2004

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