Davison V - Search Results

1

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

Shuib S, McMullan D, Rattenberry E, Barber RM, Rahman F, Zatyka M, Chapman C, Macdonald F, Latif F, Davison V, Maher ER. Shuib S, et al. Among authors: davison v. Am J Med Genet A. 2009 Oct;149A(10):2099-105. doi: 10.1002/ajmg.a.32824. Am J Med Genet A. 2009. PMID: 19760623

2

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.

Patel C, Cooper-Charles L, McMullan DJ, Walker JM, Davison V, Morton J. Patel C, et al. Among authors: davison v. Eur J Hum Genet. 2011 Jun;19(6):634-9. doi: 10.1038/ejhg.2010.238. Epub 2011 Mar 9. Eur J Hum Genet. 2011. PMID: 21386874 Free PMC article.

3

Characterization of a 3;6 translocation associated with renal cell carcinoma.

Foster RE, Abdulrahman M, Morris MR, Prigmore E, Gribble S, Ng B, Gentle D, Ready S, Weston PM, Wiesener MS, Kishida T, Yao M, Davison V, Barbero JL, Chu C, Carter NP, Latif F, Maher ER. Foster RE, et al. Among authors: davison v. Genes Chromosomes Cancer. 2007 Apr;46(4):311-7. doi: 10.1002/gcc.20403. Genes Chromosomes Cancer. 2007. PMID: 17205537 Free PMC article.

4

Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma.

Chughtai SA, Genus T, Ramani P, Dyer S, Powell JE, McMullan D, Davison V, McConville CM; UK Children's Cancer Study Group. Chughtai SA, et al. Among authors: davison v. Eur J Cancer. 2006 Aug;42(12):1826-34. doi: 10.1016/j.ejca.2006.03.016. Epub 2006 Jul 26. Eur J Cancer. 2006. PMID: 16872824

5

Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study.

Swerdlow AJ, Schoemaker MJ, Higgins CD, Wright AF, Jacobs PA; UK Clinical Cytogenetics Group. Swerdlow AJ, et al. Hum Genet. 2008 Mar;123(2):215-24. doi: 10.1007/s00439-008-0465-0. Epub 2008 Jan 15. Hum Genet. 2008. PMID: 18196273

6

Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.

Rahman N, Abidi F, Ford D, Arbour L, Rapley E, Tonin P, Barton D, Batcup G, Berry J, Cotter F, Davison V, Gerrard M, Gray E, Grundy R, Hanafy M, King D, Lewis I, Ridolfi Luethy A, Madlensky L, Mann J, O'Meara A, Oakhill T, Skolnick M, Strong L, Stratton MR, et al. Rahman N, et al. Among authors: davison v. Hum Genet. 1998 Nov;103(5):547-56. doi: 10.1007/pl00008708. Hum Genet. 1998. PMID: 9860296

7

Genomic imbalances in pediatric intracranial ependymomas define clinically relevant groups.

Dyer S, Prebble E, Davison V, Davies P, Ramani P, Ellison D, Grundy R. Dyer S, et al. Among authors: davison v. Am J Pathol. 2002 Dec;161(6):2133-41. doi: 10.1016/S0002-9440(10)64491-4. Am J Pathol. 2002. PMID: 12466129 Free PMC article.

8

Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population.

Ng A, Griffiths A, Cole T, Davison V, Griffiths M, Larkin S, Parkes SE, Mann JR, Grundy RG. Ng A, et al. Among authors: davison v. Eur J Cancer. 2007 Jun;43(9):1422-9. doi: 10.1016/j.ejca.2007.03.020. Epub 2007 May 17. Eur J Cancer. 2007. PMID: 17499987

9

Mortality in women with turner syndrome in Great Britain: a national cohort study.

Schoemaker MJ, Swerdlow AJ, Higgins CD, Wright AF, Jacobs PA; United Kingdom Clinical Cytogenetics Group. Schoemaker MJ, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4735-42. doi: 10.1210/jc.2008-1049. Epub 2008 Sep 23. J Clin Endocrinol Metab. 2008. PMID: 18812477

10

Duplication of chromosome 2 in association with ventriculomegaly - a case report.

Martin WL, Pretlove S, Mercer A, Platt CC, Roberts E, Davison V, Kilby MD. Martin WL, et al. Among authors: davison v. Prenat Diagn. 2001 Dec;21(13):1169-70. doi: 10.1002/pd.216. Prenat Diagn. 2001. PMID: 11787046

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