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Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype.
Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Hum Mol Genet. 1995 Feb;4(2):203-6. doi: 10.1093/hmg/4.2.203. Hum Mol Genet. 1995. PMID: 7757068
Study of the Huntington's disease (HD) gene CAG repeats in schizophrenic patients shows overlap of the normal and HD affected ranges but absence of correlation with schizophrenia.
Rubinsztein DC, Leggo J, Goodburn S, Crow TJ, Lofthouse R, DeLisi LE, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. J Med Genet. 1994 Sep;31(9):690-3. doi: 10.1136/jmg.31.9.690. J Med Genet. 1994. PMID: 7815437 Free PMC article.
The EUROGEM map of human chromosome 9.
Attwood J, Vergnaud G, Lush ML, Rubinsztein DC, Goudie D, Ferguson-Smith M, Povey S. Attwood J, et al. Eur J Hum Genet. 1994;2(3):220-1. Eur J Hum Genet. 1994. PMID: 7834289 No abstract available.
The EUROGEM map of human chromosome X.
Aldred MA, Flint T, Vossen R, Wakefield K, Ferguson-Smith MA, Lush M, Rubinsztein D, Kruse T, Loizedda A, Bakker B, et al. Aldred MA, et al. Eur J Hum Genet. 1994;2(3):248-9. Eur J Hum Genet. 1994. PMID: 7834303 No abstract available.
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.
Rubinsztein DC, Amos W, Leggo J, Goodburn S, Ramesar RS, Old J, Bontrop R, McMahon R, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Nat Genet. 1994 Aug;7(4):525-30. doi: 10.1038/ng0894-525. Nat Genet. 1994. PMID: 7951324
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.
Rubinsztein DC, Barton DE, Davison BC, Ferguson-Smith MA. Rubinsztein DC, et al. Hum Mol Genet. 1993 Oct;2(10):1713-5. doi: 10.1093/hmg/2.10.1713. Hum Mol Genet. 1993. PMID: 8268927 No abstract available.
Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes.
Rubinsztein DC, Leggo J, Coetzee GA, Irvine RA, Buckley M, Ferguson-Smith MA. Rubinsztein DC, et al. Hum Mol Genet. 1995 Sep;4(9):1585-90. doi: 10.1093/hmg/4.9.1585. Hum Mol Genet. 1995. PMID: 8541843
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.
Rubinsztein DC, Leggo J, Coles R, Almqvist E, Biancalana V, Cassiman JJ, Chotai K, Connarty M, Crauford D, Curtis A, Curtis D, Davidson MJ, Differ AM, Dode C, Dodge A, Frontali M, Ranen NG, Stine OC, Sherr M, Abbott MH, Franz ML, Graham CA, Harper PS, Hedreen JC, Hayden MR, et al. Rubinsztein DC, et al. Am J Hum Genet. 1996 Jul;59(1):16-22. Am J Hum Genet. 1996. PMID: 8659522 Free PMC article.
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