Robinson DO - Search Results

1

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification.

Bunyan DJ, Eccles DM, Sillibourne J, Wilkins E, Thomas NS, Shea-Simonds J, Duncan PJ, Curtis CE, Robinson DO, Harvey JF, Cross NC. Bunyan DJ, et al. Among authors: robinson do. Br J Cancer. 2004 Sep 13;91(6):1155-9. doi: 10.1038/sj.bjc.6602121. Br J Cancer. 2004. PMID: 15475941 Free PMC article.

2

Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.

Bunyan DJ, Skinner AC, Ashton EJ, Sillibourne J, Brown T, Collins AL, Cross NC, Harvey JF, Robinson DO. Bunyan DJ, et al. Among authors: robinson do. Mol Biotechnol. 2007 Feb;35(2):135-40. doi: 10.1007/BF02686108. Mol Biotechnol. 2007. PMID: 17435279

3

Multiple de novo mutations in the MECP2 gene.

Bunyan DJ, Robinson DO. Bunyan DJ, et al. Among authors: robinson do. Genet Test. 2008 Sep;12(3):373-5. doi: 10.1089/gte.2008.0012. Genet Test. 2008. PMID: 18652533

4

Influence of the MDM2 single nucleotide polymorphism SNP309 on tumour development in BRCA1 mutation carriers.

Copson ER, White HE, Blaydes JP, Robinson DO, Johnson PW, Eccles DM. Copson ER, et al. Among authors: robinson do. BMC Cancer. 2006 Mar 24;6:80. doi: 10.1186/1471-2407-6-80. BMC Cancer. 2006. PMID: 16563154 Free PMC article.

5

Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletions.

Bunyan DJ, Crolla JA, Collins AL, Robinson DO. Bunyan DJ, et al. Among authors: robinson do. Hum Genet. 1995 Jan;95(1):43-5. doi: 10.1007/BF00225072. Hum Genet. 1995. PMID: 7814024

6

Molecular analysis of x-chromosome inactivation.

Robinson DO, Harvey JF. Robinson DO, et al. Methods Mol Med. 1996;5:141-52. doi: 10.1385/0-89603-346-5:141. Methods Mol Med. 1996. PMID: 21374515

7

Identification of false-positive CBFbeta/MYH11 RT-PCR results.

Hackwell SM, Robinson DO, Harvey JF, Ross FM. Hackwell SM, et al. Among authors: robinson do. Leukemia. 1999 Oct;13(10):1617-9. doi: 10.1038/sj.leu.2401545. Leukemia. 1999. PMID: 10516764

8

Oculopharyngeal muscular dystrophy (OPMD): analysis of the PABPN1 gene expansion sequence in 86 patients reveals 13 different expansion types and further evidence for unequal recombination as the mutational mechanism.

Robinson DO, Hammans SR, Read SP, Sillibourne J. Robinson DO, et al. Hum Genet. 2005 Mar;116(4):267-71. doi: 10.1007/s00439-004-1235-2. Epub 2005 Jan 12. Hum Genet. 2005. PMID: 15645184

9

A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis.

Robinson DO, Bunyan DJ, Gabb HA, Temple IK, Yau SC. Robinson DO, et al. Hum Genet. 1997 May;99(5):658-62. doi: 10.1007/s004390050424. Hum Genet. 1997. PMID: 9150736

10

Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy.

Bunyan DJ, Robinson DO, Collins AL, Cockwell AE, Bullman HM, Whittaker PA. Bunyan DJ, et al. Among authors: robinson do. Hum Genet. 1994 May;93(5):541-4. doi: 10.1007/BF00202820. Hum Genet. 1994. PMID: 8168831

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