Murray A - Search Results

1

An investigation of FRAXA intermediate allele phenotype in a longitudinal sample.

Ennis S, Murray A, Youings S, Brightwell G, Herrick D, Ring S, Pembrey M, Morton NE, Jacobs PA. Ennis S, et al. Among authors: murray a. Ann Hum Genet. 2006 Mar;70(Pt 2):170-80. doi: 10.1111/j.1529-8817.2005.00220.x. Ann Hum Genet. 2006. PMID: 16626328

2

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.

Murray A, Macpherson JN, Pound MC, Sharrock A, Youings SA, Dennis NR, McKechnie N, Linehan P, Morton NE, Jacobs PA. Murray A, et al. Hum Mol Genet. 1997 Feb;6(2):173-84. doi: 10.1093/hmg/6.2.173. Hum Mol Genet. 1997. PMID: 9063737

3

FRAXA and FRAXE: the results of a five year survey.

Youings SA, Murray A, Dennis N, Ennis S, Lewis C, McKechnie N, Pound M, Sharrock A, Jacobs P. Youings SA, et al. Among authors: murray a. J Med Genet. 2000 Jun;37(6):415-21. doi: 10.1136/jmg.37.6.415. J Med Genet. 2000. PMID: 10851251 Free PMC article.

4

Allelic association in the FRAX region.

Ennis S, Collins A, Murray A, Macpherson JN, Morton NE. Ennis S, et al. Among authors: murray a. Ann Hum Genet. 2000 Nov;64(Pt 6):513-8. doi: 10.1017/s000348000000837x. Ann Hum Genet. 2000. PMID: 11281215

5

Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?

Ennis S, Murray A, Morton NE. Ennis S, et al. Among authors: murray a. Hum Mutat. 2001;18(1):61-9. doi: 10.1002/humu.1150. Hum Mutat. 2001. PMID: 11438994

6

Allelic association discriminates draft orders.

Ennis S, Collins A, Tapper W, Murray A, MacPherson JN, Morton NE. Ennis S, et al. Among authors: murray a. Ann Hum Genet. 2001 Sep;65(Pt 5):503-4. doi: 10.1017/s000348000100879x. Ann Hum Genet. 2001. PMID: 11811150 No abstract available.

7

Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.

Ennis S, Murray A, Brightwell G, Morton NE, Jacobs PA. Ennis S, et al. Among authors: murray a. Hum Mutat. 2007 Dec;28(12):1216-24. doi: 10.1002/humu.20600. Hum Mutat. 2007. PMID: 17674408 Free PMC article.

8

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. Eichler EE, et al. Among authors: murray a. Hum Mol Genet. 1996 Mar;5(3):319-30. doi: 10.1093/hmg/5.3.319. Hum Mol Genet. 1996. PMID: 8852655

9

FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability.

Teague JW, Morton NE, Dennis NR, Curtis G, McKechnie N, Macpherson JN, Murray A, Pound MC, Sharrock AJ, Youings SA, Jacobs PA. Teague JW, et al. Among authors: murray a. Proc Natl Acad Sci U S A. 1998 Jan 20;95(2):719-24. doi: 10.1073/pnas.95.2.719. Proc Natl Acad Sci U S A. 1998. PMID: 9435259 Free PMC article.

10

Fragile X premutation screening in women with premature ovarian failure.

Conway GS, Payne NN, Webb J, Murray A, Jacobs PA. Conway GS, et al. Among authors: murray a. Hum Reprod. 1998 May;13(5):1184-7. doi: 10.1093/humrep/13.5.1184. Hum Reprod. 1998. PMID: 9647544

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