Harper PS - Search Results

1

Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.

Harper PS, Youngman S, Anderson MA, Sarfarazi M, Quarrell O, Tanzi R, Shaw D, Wallace P, Conneally PM, Gusella JF. Harper PS, et al. J Med Genet. 1985 Dec;22(6):447-50. doi: 10.1136/jmg.22.6.447. J Med Genet. 1985. PMID: 3001311 Free PMC article.

2

Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population.

Lazarou LP, Davies F, Sarfarazi M, Coles GA, Harper PS. Lazarou LP, et al. Among authors: harper ps. J Med Genet. 1987 Aug;24(8):466-73. doi: 10.1136/jmg.24.8.466. J Med Genet. 1987. PMID: 2443703 Free PMC article.

3

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.

Snell RG, Lazarou LP, Youngman S, Quarrell OW, Wasmuth JJ, Shaw DJ, Harper PS. Snell RG, et al. Among authors: harper ps. J Med Genet. 1989 Nov;26(11):673-5. doi: 10.1136/jmg.26.11.673. J Med Genet. 1989. PMID: 2531223 Free PMC article.

4

Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8).

Quarrell OW, Youngman S, Sarfarazi M, Harper PS. Quarrell OW, et al. Among authors: harper ps. J Med Genet. 1988 Mar;25(3):191-4. doi: 10.1136/jmg.25.3.191. J Med Genet. 1988. PMID: 2895189 Free PMC article.

5

The problem of isolated cases of Huntington's disease in South Wales 1974-1984.

Quarrell OW, Tyler A, Cole G, Harper PS. Quarrell OW, et al. Among authors: harper ps. Clin Genet. 1986 Nov;30(5):433-9. doi: 10.1111/j.1399-0004.1986.tb01903.x. Clin Genet. 1986. PMID: 2948738

6

An integrated microcomputer system to maintain a genetic register for Huntington disease.

Sarfarazi M, Quarrell OW, Wolak G, Harper PS. Sarfarazi M, et al. Among authors: harper ps. Am J Med Genet. 1987 Dec;28(4):999-1006. doi: 10.1002/ajmg.1320280427. Am J Med Genet. 1987. PMID: 2961261

7

Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.

Brown CS, Pearson PL, Thomas NS, Sarfarazi M, Harper PS, Shaw DJ. Brown CS, et al. Among authors: harper ps. J Med Genet. 1985 Jun;22(3):179-81. doi: 10.1136/jmg.22.3.179. J Med Genet. 1985. PMID: 2989525 Free PMC article.

8

Studies of a DNA marker (G8) genetically linked to Huntington disease in British families.

Youngman S, Sarfarazi M, Quarrell OW, Conneally PM, Gibbons K, Harper PS, Shaw DJ, Tanzi RE, Wallace MR, Gusella JF. Youngman S, et al. Among authors: harper ps. Hum Genet. 1986 Aug;73(4):333-9. doi: 10.1007/BF00279096. Hum Genet. 1986. PMID: 3017842

9

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

Kingston HM, Thomas NS, Pearson PL, Sarfarazi M, Harper PS. Kingston HM, et al. Among authors: harper ps. J Med Genet. 1983 Aug;20(4):255-8. doi: 10.1136/jmg.20.4.255. J Med Genet. 1983. PMID: 6620324 Free PMC article.

10

Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.

Quarrell OW, Snell RG, Curtis MA, Roberts SH, Harper PS, Shaw DJ. Quarrell OW, et al. Among authors: harper ps. J Med Genet. 1991 Apr;28(4):256-9. doi: 10.1136/jmg.28.4.256. J Med Genet. 1991. PMID: 1856831 Free PMC article.

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