Harper PS - Search Results

1

Should we test children for "adult" genetic diseases?

Harper PS, Clarke A. Harper PS, et al. Lancet. 1990 May 19;335(8699):1205-6. doi: 10.1016/0140-6736(90)92713-r. Lancet. 1990. PMID: 1971046 No abstract available.

2

X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Zonana J, Clarke A, Sarfarazi M, Thomas NS, Roberts K, Marymee K, Harper PS. Zonana J, et al. Among authors: harper ps. Am J Hum Genet. 1988 Jul;43(1):75-85. Am J Hum Genet. 1988. PMID: 3163892 Free PMC article.

3

Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales. The South Wales Cystic Fibrosis Carrier Screening Research Team.

Payne Y, Williams M, Cheadle J, Stott NC, Rowlands M, Shickle D, West G, Meredith L, Goodchild M, Harper PS, Clarke A. Payne Y, et al. Among authors: harper ps. Clin Genet. 1997 Mar;51(3):153-63. doi: 10.1111/j.1399-0004.1997.tb02445.x. Clin Genet. 1997. PMID: 9137879

4

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.

Clarke A, Phillips DI, Brown R, Harper PS. Clarke A, et al. Among authors: harper ps. Arch Dis Child. 1987 Oct;62(10):989-96. doi: 10.1136/adc.62.10.989. Arch Dis Child. 1987. PMID: 2445301 Free PMC article.

5

Screening for Duchenne muscular dystrophy.

Fenton-May J, Bradley DM, Sibert JR, Smith R, Parsons EP, Harper PS, Clarke A. Fenton-May J, et al. Among authors: harper ps. Arch Dis Child. 1994 Jun;70(6):551-2. doi: 10.1136/adc.70.6.551. Arch Dis Child. 1994. PMID: 8048834 Free PMC article. No abstract available.

6

Charcot-Marie-tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2-->12.

Upadhyaya M, Roberts SH, Farnham J, MacMillan JC, Clarke A, Heath JP, Hodges IC, Harper PS. Upadhyaya M, et al. Among authors: harper ps. Hum Genet. 1993 May;91(4):392-4. doi: 10.1007/BF00217365. Hum Genet. 1993. PMID: 8500795

7

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants.

Ryan MP, French J, al-Mahdawi S, Nihoyannopoulos P, Cleland JG, Oakley CM, Harper PS, Clarke A, Davis J, Grigg L. Ryan MP, et al. Among authors: harper ps. BMJ. 1995 Apr 1;310(6983):856-9. doi: 10.1136/bmj.310.6983.856. BMJ. 1995. PMID: 7677835 Free PMC article. No abstract available.

8

Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis.

Zonana J, Sarfarazi M, Thomas NS, Clarke A, Marymee K, Harper PS. Zonana J, et al. Among authors: harper ps. J Pediatr. 1989 Mar;114(3):392-9. doi: 10.1016/s0022-3476(89)80556-6. J Pediatr. 1989. PMID: 2564048

9

Problems in genetic prediction for Huntington's disease.

Morris MJ, Tyler A, Lazarou L, Meredith L, Harper PS. Morris MJ, et al. Among authors: harper ps. Lancet. 1989 Sep 9;2(8663):601-3. doi: 10.1016/s0140-6736(89)90721-6. Lancet. 1989. PMID: 2570292

10

Adoption and genetic prediction for Huntington's disease.

Morris M, Tyler A, Harper PS. Morris M, et al. Among authors: harper ps. Lancet. 1988 Nov 5;2(8619):1069-70. doi: 10.1016/s0140-6736(88)90078-5. Lancet. 1988. PMID: 2903290

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