Williamson R - Search Results

1

Psychological and social consequences of community carrier screening programme for cystic fibrosis.

Watson EK, Mayall ES, Lamb J, Chapple J, Williamson R. Watson EK, et al. Among authors: williamson r. Lancet. 1992 Jul 25;340(8813):217-20. doi: 10.1016/0140-6736(92)90477-k. Lancet. 1992. PMID: 1353144

2

Screening for carriers of cystic fibrosis through primary health care services.

Watson EK, Mayall E, Chapple J, Dalziel M, Harrington K, Williams C, Williamson R. Watson EK, et al. Among authors: williamson r. BMJ. 1991 Aug 31;303(6801):504-7. doi: 10.1136/bmj.303.6801.504. BMJ. 1991. PMID: 1912861 Free PMC article.

3

Attitudes to carrier screening for cystic fibrosis: a survey of health care professionals, relatives of sufferers and other members of the public.

Watson EK, Williamson R, Chapple J. Watson EK, et al. Among authors: williamson r. Br J Gen Pract. 1991 Jun;41(347):237-40. Br J Gen Pract. 1991. PMID: 1931202 Free PMC article.

4

Community attitudes to cystic fibrosis carrier testing in England: a pilot study.

Williamson R, Allison ME, Bentley TJ, Lim SM, Watson E, Chapple J, Adam S, Boulton M. Williamson R, et al. Prenat Diagn. 1989 Oct;9(10):727-34. doi: 10.1002/pd.1970091008. Prenat Diagn. 1989. PMID: 2594700

5

delta F508 frequency and associated haplotypes near the cystic fibrosis locus in the Yugoslav population.

Simova L, Williams C, Efremov GD, Gordova-Muratovska A, Sustić S, Watson EK, Williamson R. Simova L, et al. Among authors: williamson r. Hum Genet. 1990 Sep;85(4):432-3. doi: 10.1007/BF02428301. Hum Genet. 1990. PMID: 1976597

6

The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families.

Watson EK, Mayall ES, Simova L, Thompson EM, Warner JO, Williamson R, Williams C. Watson EK, et al. Among authors: williamson r. Hum Genet. 1990 Sep;85(4):435-6. doi: 10.1007/BF02428303. Hum Genet. 1990. PMID: 2210766

7

The introduction of two silent mutations into a CFTR cDNA construct allows improved detection of exogenous mRNA in gene transfer experiments.

Hart SL, Mayall E, Stern M, Munkonge FM, Frost A, Huang L, Vasilliou M, Williamson R, Alton EW, Coutelle C. Hart SL, et al. Among authors: williamson r. Hum Mol Genet. 1995 Sep;4(9):1597-602. doi: 10.1093/hmg/4.9.1597. Hum Mol Genet. 1995. PMID: 8541845

8

A report on CF carrier frequency among men with infertility owing to congenital absence of the vas deferens.

Williams C, Mayall ES, Williamson R, Hirsh A, Cookson H. Williams C, et al. Among authors: williamson r. J Med Genet. 1993 Nov;30(11):973. doi: 10.1136/jmg.30.11.973-a. J Med Genet. 1993. PMID: 8301660 Free PMC article. No abstract available.

9

A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.

Wainwright B, Farrall M, Watson E, Williamson R. Wainwright B, et al. Among authors: williamson r. J Med Genet. 1986 Oct;23(5):417-20. doi: 10.1136/jmg.23.5.417. J Med Genet. 1986. PMID: 3783618 Free PMC article.

10

Universal community carrier screening for cystic fibrosis?

Williamson R. Williamson R. Nat Genet. 1993 Mar;3(3):195-201. doi: 10.1038/ng0393-195. Nat Genet. 1993. PMID: 8485573 Review.

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