Clarke A - Search Results

1

Should we test children for "adult" genetic diseases?

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

2

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.

Clarke A, Phillips DI, Brown R, Harper PS. Clarke A, et al. 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.

3

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: clarke a. Am J Hum Genet. 1988 Jul;43(1):75-85. Am J Hum Genet. 1988. PMID: 3163892 Free PMC article.

4

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: clarke a. Clin Genet. 1997 Mar;51(3):153-63. doi: 10.1111/j.1399-0004.1997.tb02445.x. Clin Genet. 1997. PMID: 9137879

5

A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer.

Gray J, Brain K, Norman P, Anglim C, France L, Barton G, Branston L, Parsons E, Clarke A, Sampson J, Roberts E, Newcombe R, Cohen D, Rogers C, Mansel R, Harper P. Gray J, et al. Among authors: clarke a. J Med Genet. 2000 Mar;37(3):192-6. doi: 10.1136/jmg.37.3.192. J Med Genet. 2000. PMID: 10699055 Free PMC article. Clinical Trial.

6

Why do women attend familial breast cancer clinics?

Brain K, Gray J, Norman P, Parsons E, Clarke A, Rogers C, Mansel R, Harper P. Brain K, et al. Among authors: clarke a. J Med Genet. 2000 Mar;37(3):197-202. doi: 10.1136/jmg.37.3.197. J Med Genet. 2000. PMID: 10699056 Free PMC article.

7

Randomized trial of a specialist genetic assessment service for familial breast cancer.

Brain K, Gray J, Norman P, France E, Anglim C, Barton G, Parsons E, Clarke A, Sweetland H, Tischkowitz M, Myring J, Stansfield K, Webster D, Gower-Thomas K, Daoud R, Gateley C, Monypenny I, Singhal H, Branston L, Sampson J, Roberts E, Newcombe R, Cohen D, Rogers C, Mansel R, Harper P. Brain K, et al. Among authors: clarke a. J Natl Cancer Inst. 2000 Aug 16;92(16):1345-51. doi: 10.1093/jnci/92.16.1345. J Natl Cancer Inst. 2000. PMID: 10944557 Clinical Trial.

8

Genetic Testing Considerations in Breast Cancer Patients.

France L, Gray J, Elwyn G, Tischkowitz M, Brain K, Sampson J, Anglim C, Clarke A, Parsons E, Sweetland H, Mansel R, Barrett-Lee P, Harper P. France L, et al. Among authors: clarke a. J Genet Couns. 1999 Oct;8(5):289-99. doi: 10.1023/A:1022982232213. J Genet Couns. 1999. PMID: 26142375

9

Genetic testing for hypertrophic cardiomyopathy.

Clarke A, Harper P. Clarke A, et al. N Engl J Med. 1992 Oct 15;327(16):1175-6. doi: 10.1056/NEJM199210153271616. N Engl J Med. 1992. PMID: 1528221 No abstract available.

10

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: clarke a. Hum Genet. 1993 May;91(4):392-4. doi: 10.1007/BF00217365. Hum Genet. 1993. PMID: 8500795

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

3,817 results

Search Page