Harris R - Search Results

1

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.

2

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

3

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.

4

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.

5

Testing for cystic fibrosis using allelic association.

Ivinson AJ, Read AP, Harris R, Super M, Schwarz M, Clayton Smith J, Elles R. Ivinson AJ, et al. Among authors: harris r. J Med Genet. 1989 Jul;26(7):426-30. doi: 10.1136/jmg.26.7.426. J Med Genet. 1989. PMID: 2746614 Free PMC article.

6

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.

7

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.

8

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy.

Lunt PW, Cumming WJ, Kingston H, Read AP, Mountford RC, Mahon M, Harris R. Lunt PW, et al. Among authors: harris r. Lancet. 1989 Jan 7;1(8628):46-7. doi: 10.1016/s0140-6736(89)91704-2. Lancet. 1989. PMID: 2563028 No abstract available.

9

Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.

Donnai D, Kerzin-Storrar L, Harris R. Donnai D, et al. Among authors: harris r. J Med Genet. 1987 Feb;24(2):84-7. doi: 10.1136/jmg.24.2.84. J Med Genet. 1987. PMID: 3560172 Free PMC article.

10

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.

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