Deane, A, Fraser, R, Horowitz, M, Burgstad, C, Besanko, L, Finnis, M, ...
No abstract available.
McKenzie, O., Ponte, I., Mangelsdorf, M., Finnis, M., Colasante, G., Shoubridge, C., ...
Aristaless-related homeobox gene (ARX) is an important paired-type homeobox gene involved in the development of human brain. The ARX gene mutations are a significant contributor to various forms of...
Common chromosomal fragile site FRA16D mutation in cancer cells (2005)
Finnis, M., Dayan, S., Hobson, L., Chenevix-Trench, G., Friend, K. L., 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, M., Dayan, S., Hobson, L., Chenevix-Trench, G., Friend, K. L., 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...
Stepp, ML, Cason, AL, Finnis, M, Mangelsdorf, M, Holinski-Feder, E, Macgregor, D, ...
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...
Stepp, ML, Cason, AL, Finnis, M, Mangelsdorf, M, Holinski-Feder, E, Macgregor, D, ...
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...
AFX mutations frequently cause X-linked mental retardation. (2002)
Mangelsdorf, ME, Finnis, M, Hobson, L, Hodgson, B, Turner, G, Partington, M, ...
AFX mutations frequently cause X-linked mental retardation. (2002)
Mangelsdorf, ME, Finnis, M, Hobson, L, Hodgson, B, Turner, G, Partington, M, ...
Chromosomal fragile site FRA16D and DNA instability in cancer (2000)
Mangelsdorf, M, Ried, K, Woollatt, E, Dayan, S, Eyre, H, Finnis, M, ...
It has been proposed that common aphidicolin-inducible fragile sites, in general, predispose to specific chromosomal breakage associated with deletion, amplification, and/or translocation in certain...
Ried, K, Finnis, M, Hobson, L, Mangelsdorf, M, Dayan, S, Nancarrow, JK, ...
Fluorescence in situ hybridization of a tile path of DNA subclones has previously enabled the cytogenetic definition of the minimal DNA sequence which spans the FRA16D common chromosomal fragile...
Chromosomal fragile site FRA16D and DNA instability in cancer (2000)
Mangelsdorf, M, Ried, K, Woollatt, E, Dayan, S, Eyre, H, Finnis, M, ...
It has been proposed that common aphidicolin-inducible fragile sites, in general, predispose to specific chromosomal breakage associated with deletion, amplification, and/or translocation in certain...
Ried, K, Finnis, M, Hobson, L, Mangelsdorf, M, Dayan, S, Nancarrow, JK, ...
Fluorescence in situ hybridization of a tile path of DNA subclones has previously enabled the cytogenetic definition of the minimal DNA sequence which spans the FRA16D common chromosomal fragile...