Harper PS - Search Results

1

A DNA probe, D5 [D4S90] mapping to human chromosome 4p16.3.

Youngman S, Shaw DJ, Gusella JF, MacDonald M, Stanbridge EJ, Wasmuth J, Harper PS. Youngman S, et al. Among authors: harper ps. Nucleic Acids Res. 1988 Feb 25;16(4):1648. doi: 10.1093/nar/16.4.1648. Nucleic Acids Res. 1988. PMID: 2894638 Free PMC article.

2

Myotonic dystrophy: advances in molecular genetics.

Shaw DJ, Harper PS. Shaw DJ, et al. Among authors: harper ps. Neuromuscul Disord. 1992;2(4):241-3. doi: 10.1016/0960-8966(92)90055-b. Neuromuscul Disord. 1992. PMID: 1362366 No abstract available.

3

Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders.

MacMillan JC, Myring J, Harley HG, Reardon W, Harper PS, Shaw DJ. MacMillan JC, et al. Among authors: harper ps. Neuromuscul Disord. 1992;2(5-6):405-11. doi: 10.1016/s0960-8966(06)80012-x. Neuromuscul Disord. 1992. PMID: 1363747

4

Identification of new DNA markers close to the myotonic dystrophy locus.

Brook JD, Harley HG, Walsh KV, Rundle SA, Siciliano MJ, Harper PS, Shaw DJ. Brook JD, et al. Among authors: harper ps. J Med Genet. 1991 Feb;28(2):84-8. doi: 10.1136/jmg.28.2.84. J Med Genet. 1991. PMID: 1672160 Free PMC article.

5

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Walsh KV, Harley HG, Brook JD, Rundle SA, Sarfarazi M, Harper PS, Shaw DJ. Walsh KV, et al. Among authors: harper ps. Hum Genet. 1990 Aug;85(3):305-10. doi: 10.1007/BF00206751. Hum Genet. 1990. PMID: 1975560

6

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.

7

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.

8

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.

9

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.

10

Molecular basis of neurofibromatosis type 1 (NF1): mutation analysis and polymorphisms in the NF1 gene.

Upadhyaya M, Shaw DJ, Harper PS. Upadhyaya M, et al. Among authors: harper ps. Hum Mutat. 1994;4(2):83-101. doi: 10.1002/humu.1380040202. Hum Mutat. 1994. PMID: 7981724 Review.

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