Dearlove A - Search Results

1

A high-resolution microsatellite map of the mouse genome.

Rhodes M, Straw R, Fernando S, Evans A, Lacey T, Dearlove A, Greystrong J, Walker J, Watson P, Weston P, Kelly M, Taylor D, Gibson K, Mundy C, Bourgade F, Poirier C, Simon D, Brunialti AL, Montagutelli X, Gu'enet JL, Haynes A, Brown SD. Rhodes M, et al. Among authors: dearlove a. Genome Res. 1998 May;8(5):531-42. doi: 10.1101/gr.8.5.531. Genome Res. 1998. PMID: 9582196 Free article.

2

High-throughput microsatellite analysis using fluorescent dUTPs for high-resolution genetic mapping of the mouse genome.

Rhodes M, Dearlove A, Straw R, Fernando S, Evans A, Greener M, Lacey T, Kelly M, Gibson K, Brown SD, Mundy C. Rhodes M, et al. Among authors: dearlove a. Genome Res. 1997 Jan;7(1):81-6. doi: 10.1101/gr.7.1.81. Genome Res. 1997. PMID: 9037606 Free article.

3

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.

Reid E, Dearlove AM, Rhodes M, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. Am J Hum Genet. 1999 Sep;65(3):757-63. doi: 10.1086/302555. Am J Hum Genet. 1999. PMID: 10441583 Free PMC article.

4

Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.

Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC. Reid E, et al. Among authors: dearlove am. Neurology. 1999 Nov 10;53(8):1844-9. doi: 10.1212/wnl.53.8.1844. Neurology. 1999. PMID: 10563637

5

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping.

Ohadi M, Lalloz MR, Sham P, Zhao J, Dearlove AM, Shiach C, Kinsey S, Rhodes M, Layton DM. Ohadi M, et al. Among authors: dearlove am. Am J Hum Genet. 1999 Jan;64(1):165-71. doi: 10.1086/302187. Am J Hum Genet. 1999. PMID: 9915955 Free PMC article.

6

A genome-wide family-based linkage study of coeliac disease.

King AL, Yiannakou JY, Brett PM, Curtis D, Morris MA, Dearlove AM, Rhodes M, Rosen-Bronson S, Mathew C, Ellis HJ, Ciclitira PJ. King AL, et al. Among authors: dearlove am. Ann Hum Genet. 2000 Nov;64(Pt 6):479-90. doi: 10.1046/j.1469-1809.2000.6460479.x. Ann Hum Genet. 2000. PMID: 11281212

7

Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus.

Ragge NK, Hartley C, Dearlove AM, Walker J, Russell-Eggitt I, Harris CM. Ragge NK, et al. Among authors: dearlove am. J Med Genet. 2003 Jan;40(1):37-41. doi: 10.1136/jmg.40.1.37. J Med Genet. 2003. PMID: 12525540 Free PMC article.

8

Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.

Brockington M, Sewry CA, Herrmann R, Naom I, Dearlove A, Rhodes M, Topaloglu H, Dubowitz V, Voit T, Muntoni F. Brockington M, et al. Among authors: dearlove a. Am J Hum Genet. 2000 Feb;66(2):428-35. doi: 10.1086/302775. Am J Hum Genet. 2000. PMID: 10677302 Free PMC article.

9

High throughput genotyping technologies.

Dearlove AM. Dearlove AM. Brief Funct Genomic Proteomic. 2002 Jul;1(2):139-50. doi: 10.1093/bfgp/1.2.139. Brief Funct Genomic Proteomic. 2002. PMID: 15239900 Review.

10

Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13.

Curtis D, Brett P, Dearlove AM, McQuillin A, Kalsi G, Robertson MM, Gurling HM. Curtis D, et al. Among authors: dearlove am. Psychiatr Genet. 2004 Jun;14(2):83-7. doi: 10.1097/01.ypg.0000107927.32051.f5. Psychiatr Genet. 2004. PMID: 15167693

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