Barton DE - Search Results

1

Normal CAG and CCG repeats in the Huntington's disease genes of Parkinson's disease patients.

Rubinsztein DC, Leggo J, Goodburn S, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: barton de. Am J Med Genet. 1995 Apr 24;60(2):109-10. doi: 10.1002/ajmg.1320600205. Am J Med Genet. 1995. PMID: 7485243

2

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. Among authors: barton de. 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.

3

Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.

Rubinsztein DC, Leggo J, Amos W, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: barton de. Hum Mol Genet. 1994 Nov;3(11):2031-5. Hum Mol Genet. 1994. PMID: 7874122

4

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. Among authors: barton de. Nat Genet. 1994 Aug;7(4):525-30. doi: 10.1038/ng0894-525. Nat Genet. 1994. PMID: 7951324

5

Issues in Huntington's disease testing.

Rubinsztein DC, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: barton de. Q J Med. 1994 Feb;87(2):71-3. Q J Med. 1994. PMID: 8153290

6

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. Among authors: barton de. 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.

7

Instability of normal (CTG)n alleles in the DM kinase gene.

Dow DJ, Rubinsztein DC, Yates JR, Barton DE, Ferguson-Smith MA. Dow DJ, et al. Among authors: barton de. J Med Genet. 1997 Oct;34(10):871-3. doi: 10.1136/jmg.34.10.871. J Med Genet. 1997. PMID: 9350827 Free PMC article.

8

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. Among authors: barton de. Hum Mol Genet. 1995 Feb;4(2):203-6. doi: 10.1093/hmg/4.2.203. Hum Mol Genet. 1995. PMID: 7757068

9

Site of (CCG) polymorphism in the HD gene.

Rubinsztein DC, Leggo J, Barton DE, Ferguson-Smith MA. Rubinsztein DC, et al. Among authors: barton de. Nat Genet. 1993 Nov;5(3):214-5. doi: 10.1038/ng1193-214. Nat Genet. 1993. PMID: 8275082 No abstract available.

10

Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A families.

McMahon R, Mulligan LM, Healey CS, Payne SJ, Ponder M, Ferguson-Smith MA, Barton DE, Ponder BA. McMahon R, et al. Among authors: barton de. Hum Mol Genet. 1994 Apr;3(4):643-6. doi: 10.1093/hmg/3.4.643. Hum Mol Genet. 1994. PMID: 7915166

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