Merran Finnis

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L, Cason, A Lauren, Finnis, Merran, Mangelsdorf, Marie, Holinski-Feder, Elke, Macgregor, David, ...

Abstract Background X-linked mental retardation (XLMR) is the leading cause of mental retardation in males. Mutations in the ARX gene in Xp22.1 have been found in numerous families with both...

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L., Cason, A. Lauren, Finnis, Merran, Mangelsdorf, Marie Elise, Holinski-Feder, Elke, Macgregor, David, ...

© 2005 Stepp et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),...

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L., Cason, A. Lauren, Finnis, Merran, Mangelsdorf, Marie Elise, Holinski-Feder, Elke, Macgregor, David, ...

© 2005 Stepp et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),...

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene (2005)

Stepp, Monica L., Cason, A. Lauren, Finnis, Merran, Mangelsdorf, Marie, Holinski-Feder, Elke, Macgregor, David, ...

Background: X-linked mental retardation (XLMR) is the leading cause of mental retardation in males. Mutations in the ARX gene in Xp22.1 have been found in numerous families with both nonsyndromic and...

Common chromosomal fragile site FRA16D mutation in cancer cells (2005)

Finnis, Merran, Dayan, Sonia, Hobson, Lynne, Chenevix-Trench, Georgia, Friend, Kathryn, Ried, Karin, ...

Neither the molecular basis for common fragile site DNA instability nor the contribution of this form of chromosomal instability to cancer is clearly understood. Fragile site FRA16D (16q23.2) is...

Common chromosomal fragile site FRA16D mutation in cancer cells (2005)

Finnis, Merran, Dayan, Sonia, Hobson, Lynne, Chenevix-Trench, Georgia, Friend, Kathryn, Ried, Karin, ...

Neither the molecular basis for common fragile site DNA instability, nor the contribution of this form of chromosomal instability to cancer, are clearly understood. Fragile site FRA16D (16q23.2) is...

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein (2004)

Sarafidou, Theologia, Kahl, Christina, Martinez-Garay, Isabel, Marie Mangelsdorf,, Stefan Gesk,, Baker, Elizabeth, ...

Fragile sites appear visually as nonstaining gaps on chromosomes that are inducible by specific cell culture conditions. Expansion of CGG/ CCG repeats has been shown to be the molecular basis of all...