Harper PS - Search Results

1

Huntington's disease: prediction and prevention.

Harper PS, Quarrell OW, Youngman S. Harper PS, et al. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):285-98. doi: 10.1098/rstb.1988.0050. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900522 Review.

2

Exclusion testing in pregnancy for Huntington's disease.

Tyler A, Quarrell OW, Lazarou LP, Meredith AL, Harper PS. Tyler A, et al. Among authors: harper ps. J Med Genet. 1990 Aug;27(8):488-95. doi: 10.1136/jmg.27.8.488. J Med Genet. 1990. PMID: 2145437 Free PMC article.

3

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

Robbins C, Theilmann J, Youngman S, Haines J, Altherr MJ, Harper PS, Payne C, Junker A, Wasmuth J, Hayden MR. Robbins C, et al. Among authors: harper ps. Am J Hum Genet. 1989 Mar;44(3):422-5. Am J Hum Genet. 1989. PMID: 2521771 Free PMC article.

4

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.

5

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.

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

Population studies of Huntington's disease in Wales.

Quarrell OW, Tyler A, Jones MP, Nordin M, Harper PS. Quarrell OW, et al. Among authors: harper ps. Clin Genet. 1988 Mar;33(3):189-95. doi: 10.1111/j.1399-0004.1988.tb03436.x. Clin Genet. 1988. PMID: 2966022

8

Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.

MacMillan JC, Morrison PJ, Nevin NC, Shaw DJ, Harper PS, Quarrell OW, Snell RG. MacMillan JC, et al. Among authors: harper ps. J Med Genet. 1993 Dec;30(12):1012-3. doi: 10.1136/jmg.30.12.1012. J Med Genet. 1993. PMID: 8133497 Free PMC article.

9

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.

10

Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA marker.

Quarrell OW, Meredith AL, Tyler A, Youngman S, Upadhyaya M, Harper PS. Quarrell OW, et al. Among authors: harper ps. Lancet. 1987 Jun 6;1(8545):1281-3. doi: 10.1016/s0140-6736(87)90541-1. Lancet. 1987. PMID: 2884411

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