Barton DE - Search Results

1

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Joyce JA, Davies R, Gareth D, Evans R, Ponder BA, Barton DE, Maher ER. Froggatt NJ, et al. Among authors: barton de. Lancet. 1995 Mar 18;345(8951):727. doi: 10.1016/s0140-6736(95)90900-1. Lancet. 1995. PMID: 7885145 No abstract available.

2

Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

Froggatt NJ, Koch J, Davies R, Evans DG, Clamp A, Quarrell OW, Weissenbach J, Hodgson SV, Ponder BA, Barton DE, et al. Froggatt NJ, et al. Among authors: barton de. J Med Genet. 1995 May;32(5):352-7. doi: 10.1136/jmg.32.5.352. J Med Genet. 1995. PMID: 7616541 Free PMC article.

3

Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancer.

Joyce JA, Froggatt NJ, Davies R, Evans DG, Trembath R, Barton DE, Maher ER. Joyce JA, et al. Among authors: barton de. Clin Genet. 1995 Dec;48(6):299-303. doi: 10.1111/j.1399-0004.1995.tb04113.x. Clin Genet. 1995. PMID: 8835324

4

Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Barton D, Jennings A, Fellows IW, Ponder MA, Ponder BA, Benjamin C, Harris R, et al. Maher ER, et al. J Neurol Sci. 1990 Dec;100(1-2):27-30. doi: 10.1016/0022-510x(90)90008-b. J Neurol Sci. 1990. PMID: 1982450

5

Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.

Slatter RE, Elliott M, Welham K, Carrera M, Schofield PN, Barton DE, Maher ER. Slatter RE, et al. Among authors: barton de. J Med Genet. 1994 Oct;31(10):749-53. doi: 10.1136/jmg.31.10.749. J Med Genet. 1994. PMID: 7837249 Free PMC article.

6

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

7

Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma.

Irving RM, Moffat DA, Hardy DG, Barton DE, Xuereb JH, Maher ER. Irving RM, et al. Among authors: barton de. Hum Mol Genet. 1994 Feb;3(2):347-50. doi: 10.1093/hmg/3.2.347. Hum Mol Genet. 1994. PMID: 8004107

8

A molecular, clinical, and immunohistochemical study of vestibular schwannoma.

Irving RM, Moffat DA, Hardy DG, Barton DE, Xuereb JH, Holland FJ, Maher ER. Irving RM, et al. Among authors: barton de. Otolaryngol Head Neck Surg. 1997 Apr;116(4):426-30. doi: 10.1016/S0194-59989770289-4. Otolaryngol Head Neck Surg. 1997. PMID: 9141389

9

Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma.

Harada T, Irving RM, Xuereb JH, Barton DE, Hardy DG, Moffat DA, Maher ER. Harada T, et al. Among authors: barton de. J Neurosurg. 1996 May;84(5):847-51. doi: 10.3171/jns.1996.84.5.0847. J Neurosurg. 1996. PMID: 8622160

10

Cystic fibrosis diagnosed by molecular genetic investigation in the mother of a patient with cystic fibrosis.

Gregory GA, Woolf DA, McMahon R, Maher ER, Barton DE. Gregory GA, et al. Among authors: barton de. Thorax. 1997 Jan;52(1):96-7. Thorax. 1997. PMID: 9039249 Free article. No abstract available.

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