Harris R - Search Results

1

Bridging markers defining the map position of X linked hypophosphataemic rickets.

Thakker RV, Read AP, Davies KE, Whyte MP, Weksberg R, Glorieux F, Davies M, Mountford RC, Harris R, King A, et al. Thakker RV, et al. Among authors: harris r. J Med Genet. 1987 Dec;24(12):756-60. doi: 10.1136/jmg.24.12.756. J Med Genet. 1987. PMID: 2828625 Free PMC article.

2

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.

Read AP, Thakker RV, Davies KE, Mountford RC, Brenton DP, Davies M, Glorieux F, Harris R, Hendy GN, King A, et al. Read AP, et al. Among authors: harris r. Hum Genet. 1986 Jul;73(3):267-70. doi: 10.1007/BF00401242. Hum Genet. 1986. PMID: 3015770

3

A register based system for gene tracking in Duchenne muscular dystrophy.

Read AP, Kerzin-Storrar L, Mountford RC, Elles RG, Harris R. Read AP, et al. Among authors: harris r. J Med Genet. 1986 Dec;23(6):581-6. doi: 10.1136/jmg.23.6.581. J Med Genet. 1986. PMID: 2879930 Free PMC article.

4

Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.

McKeown C, Read AP, Dodge A, Stecko O, Mercer A, Harris R. McKeown C, et al. Among authors: harris r. J Med Genet. 1987 Jul;24(7):410-2. doi: 10.1136/jmg.24.7.410. J Med Genet. 1987. PMID: 3612716 Free PMC article.

5

Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register.

Elles RG, Hodgkinson KA, Mallick NP, O'Donoghue DJ, Read AP, Rimmer S, Watters EA, Harris R. Elles RG, et al. Among authors: harris r. J Med Genet. 1994 Feb;31(2):115-20. doi: 10.1136/jmg.31.2.115. J Med Genet. 1994. PMID: 8182715 Free PMC article.

6

Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?

Elles RG, Read AP, Hodgkinson KA, Watters A, Harris R. Elles RG, et al. Among authors: harris r. J Med Genet. 1990 Jul;27(7):413-7. doi: 10.1136/jmg.27.7.413. J Med Genet. 1990. PMID: 1975629 Free PMC article.

7

Patterns of exon deletions in Duchenne and Becker muscular dystrophy.

Read AP, Mountford RC, Forrest SM, Kenwrick SJ, Davies KE, Harris R. Read AP, et al. Among authors: harris r. Hum Genet. 1988 Oct;80(2):152-6. doi: 10.1007/BF00702859. Hum Genet. 1988. PMID: 3169738

8

Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Foy C, Newton V, Wellesley D, Harris R, Read AP. Foy C, et al. Among authors: harris r. Am J Hum Genet. 1990 Jun;46(6):1017-23. Am J Hum Genet. 1990. PMID: 2339698 Free PMC article.

9

New DNA markers in the Huntington's disease gene candidate region.

Lin CS, Altherr M, Bates G, Whaley WL, Read AP, Harris R, Lehrach H, Wasmuth JJ, Gusella JF, MacDonald ME. Lin CS, et al. Among authors: harris r. Somat Cell Mol Genet. 1991 Sep;17(5):481-8. doi: 10.1007/BF01233172. Somat Cell Mol Genet. 1991. PMID: 1684879

10

Molecular genetics in the National Health Service in Britain.

Harris R, Elles R, Craufurd D, Dodge A, Ivinson A, Hodgkinson K, Mountford R, Schwartz M, Strachan T, Read A. Harris R, et al. J Med Genet. 1989 Apr;26(4):219-25. doi: 10.1136/jmg.26.4.219. J Med Genet. 1989. PMID: 2523972 Free PMC article.

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