Evans DG - Search Results

1

Bilateral vestibular schwannomas in older patients: NF2 or chance?

Evans DG, Freeman S, Gokhale C, Wallace A, Lloyd SK, Axon P, Ward CL, Rutherford S, King A, Huson SM, Ramsden RT; Manchester NF2 service. Evans DG, et al. J Med Genet. 2015 Jun;52(6):422-4. doi: 10.1136/jmedgenet-2014-102973. Epub 2015 Feb 27. J Med Genet. 2015. PMID: 25725045

2

A genetic register for von Hippel-Lindau disease.

Maddock IR, Moran A, Maher ER, Teare MD, Norman A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG. Maddock IR, et al. Among authors: evans dg. J Med Genet. 1996 Feb;33(2):120-7. doi: 10.1136/jmg.33.2.120. J Med Genet. 1996. PMID: 8929948 Free PMC article.

3

Microsatellite instability in early onset and familial colorectal cancer.

Brassett C, Joyce JA, Froggatt NJ, Williams G, Furniss D, Walsh S, Miller R, Evans DG, Maher ER. Brassett C, et al. Among authors: evans dg. J Med Genet. 1996 Dec;33(12):981-5. doi: 10.1136/jmg.33.12.981. J Med Genet. 1996. PMID: 9004127 Free PMC article.

4

An evaluation of common breast cancer gene mutations in a population of Ashkenazi Jews.

Lalloo F, Cochrane S, Bulman B, Varley J, Elles R, Howell A, Evans DG. Lalloo F, et al. Among authors: evans dg. J Med Genet. 1998 Jan;35(1):10-2. doi: 10.1136/jmg.35.1.10. J Med Genet. 1998. PMID: 9475087 Free PMC article.

5

Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.

Evans DG, Trueman L, Wallace A, Collins S, Strachan T. Evans DG, et al. J Med Genet. 1998 Jun;35(6):450-5. doi: 10.1136/jmg.35.6.450. J Med Genet. 1998. PMID: 9643284 Free PMC article.

6

Somatic mosaicism: a common cause of classic disease in tumor-prone syndromes? Lessons from type 2 neurofibromatosis.

Evans DG, Wallace AJ, Wu CL, Trueman L, Ramsden RT, Strachan T. Evans DG, et al. Am J Hum Genet. 1998 Sep;63(3):727-36. doi: 10.1086/512074. Am J Hum Genet. 1998. PMID: 9718334 Free PMC article.

7

Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.

Wu CL, Thakker N, Neary W, Black G, Lye R, Ramsden RT, Read AP, Evans DG. Wu CL, et al. Among authors: evans dg. J Med Genet. 1998 Dec;35(12):973-7. doi: 10.1136/jmg.35.12.973. J Med Genet. 1998. PMID: 9863591 Free PMC article.

8

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer.

Froggatt NJ, Green J, Brassett C, Evans DG, Bishop DT, Kolodner R, Maher ER. Froggatt NJ, et al. Among authors: evans dg. J Med Genet. 1999 Feb;36(2):97-102. J Med Genet. 1999. PMID: 10051005 Free PMC article.

9

A clinical study of type 1 neurofibromatosis in north west England.

McGaughran JM, Harris DI, Donnai D, Teare D, MacLeod R, Westerbeek R, Kingston H, Super M, Harris R, Evans DG. McGaughran JM, et al. Among authors: evans dg. J Med Genet. 1999 Mar;36(3):197-203. J Med Genet. 1999. PMID: 10204844 Free PMC article.

10

Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma.

Evans DG, Lye R, Neary W, Black G, Strachan T, Wallace A, Ramsden RT. Evans DG, et al. J Neurol Neurosurg Psychiatry. 1999 Jun;66(6):764-7. doi: 10.1136/jnnp.66.6.764. J Neurol Neurosurg Psychiatry. 1999. PMID: 10329751 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,362 results

Search Page

Filters