Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence
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Ronald Bontrop | David E. Barton | William Amos | Malcolm A. Ferguson-Smith | John Old | D. Rubinsztein | D. Barton | M. Ferguson-Smith | R. Bontrop | R. Ramesar | W. Amos | J. Leggo | R. Mcmahon | David C. Rubinsztein | J. Old | S. Goodburn | Jayne Leggo | Sandy Goodburn | Rajkumar S. Ramesar | Robert McMahon
[1] M. Hayden,et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease , 1993, Nature Genetics.
[2] D. Rubinsztein,et al. Site of (CCG) polymorphism in the HD gene , 1993, Nature Genetics.
[3] M. MacDonald,et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease , 1993, Nature Genetics.
[4] M. Porteous,et al. A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. , 1993, Journal of medical genetics.
[5] J. Maddox. Triplet repeat genes raise questions , 1994, Nature.
[6] D. Brock,et al. A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes. , 1993, Molecular and cellular probes.
[7] D. Rubinsztein,et al. Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number. , 1993, Human molecular genetics.
[8] L. Surh,et al. Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy. , 1993, Genomics.
[9] Manish S. Shah,et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes , 1993, Cell.
[10] L. Peltonen,et al. Meiotic drive at the myotonic dystrophy locus? , 1994, Nature Genetics.
[11] J. Gusella,et al. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease , 1993, Nature genetics.
[12] O. Riess,et al. Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease. , 1993, Human molecular genetics.
[13] J. Penney,et al. Trinucleotide repeat length instability and age of onset in Huntington's disease , 1993, Nature Genetics.
[14] M. Lathrop,et al. The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence. , 1991, Genomics.
[15] R. Bontrop,et al. Major histocompatibility complex class II haplotypes in a breeding colony of chimpanzees (Pan troglodytes). , 1993, Tissue antigens.
[16] M. Hayden,et al. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects , 1993, Nature genetics.
[17] H. Lange,et al. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene. , 1993, Human molecular genetics.