Bourn D - Search Results

1

An intron-containing tRNAArg gene within a large cluster of human tRNA genes.

Bourn D, Carr T, Livingstone D, McLaren A, Goddard JP. Bourn D, et al. DNA Seq. 1994;5(2):83-92. doi: 10.3109/10425179409039709. DNA Seq. 1994. PMID: 7703509

2

Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1.

Morrison N, Goddard JP, Ledbetter DH, Boyd E, Bourn D, Connor JM. Morrison N, et al. Among authors: bourn d. Hum Genet. 1991 Jun;87(2):226-30. doi: 10.1007/BF00204190. Hum Genet. 1991. PMID: 2066114

3

Characterization of a human tRNA gene cluster.

Bourn D, Carr T, Livingstone D, McLaren A, Goddard JP. Bourn D, et al. Biochem Soc Trans. 1990 Aug;18(4):602. doi: 10.1042/bst0180602. Biochem Soc Trans. 1990. PMID: 2276459 No abstract available.

4

Serendipitous amplification by the polymerase chain reaction (PCR) of two adjacent tRNA(Gln)UUG) genes on target human genomic DNA.

Bourn D, Goddard JP. Bourn D, et al. Nucleic Acids Res. 1990 Dec 25;18(24):7442. doi: 10.1093/nar/18.24.7442. Nucleic Acids Res. 1990. PMID: 2259635 Free PMC article. No abstract available.

5

Dinucleotide repeat polymorphism at the NF2 gene.

Bourn D, Strachan T. Bourn D, et al. Hum Mol Genet. 1994 Oct;3(10):1914. doi: 10.1093/hmg/3.10.1914. Hum Mol Genet. 1994. PMID: 7849731 No abstract available.

6

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene.

Bourn D, Carter SA, Mason S, Gareth D, Evans R, Strachan T. Bourn D, et al. Hum Mol Genet. 1994 May;3(5):813-6. doi: 10.1093/hmg/3.5.813. Hum Mol Genet. 1994. PMID: 8081368

7

Highly polymorphic dinucleotide repeat at the NF2 gene.

Bourn D, Strachan T. Bourn D, et al. Hum Genet. 1995 Jun;95(6):712. doi: 10.1007/BF00209494. Hum Genet. 1995. PMID: 7789960

8

Eleven novel mutations in the NF2 tumour suppressor gene.

Bourn D, Evans G, Mason S, Tekes S, Trueman L, Strachan T. Bourn D, et al. Hum Genet. 1995 May;95(5):572-4. doi: 10.1007/BF00223872. Hum Genet. 1995. PMID: 7759081

9

H4 acetylation, XIST RNA and replication timing are coincident and define x;autosome boundaries in two abnormal X chromosomes.

Keohane AM, Barlow AL, Waters J, Bourn D, Turner BM. Keohane AM, et al. Among authors: bourn d. Hum Mol Genet. 1999 Feb;8(2):377-83. doi: 10.1093/hmg/8.2.377. Hum Mol Genet. 1999. PMID: 9931347

10

Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data.

Aitken S, Firth HV, McRae J, Halachev M, Kini U, Parker MJ, Lees MM, Lachlan K, Sarkar A, Joss S, Splitt M, McKee S, Németh AH, Scott RH, Wright CF, Marsh JA, Hurles ME, FitzPatrick DR; DDD Study. Aitken S, et al. Am J Hum Genet. 2019 Nov 7;105(5):933-946. doi: 10.1016/j.ajhg.2019.09.015. Epub 2019 Oct 10. Am J Hum Genet. 2019. PMID: 31607427 Free PMC article.

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