Craufurd D - Search Results

1

BRCA1/2 predictive testing: a study of uptake in two centres.

Brooks L, Lennard F, Shenton A, Lalloo F, Ambus I, Ardern-Jones A, Belk R, Kerr B, Craufurd D, Eeles R, Gareth Evans D. Brooks L, et al. Among authors: craufurd d. Eur J Hum Genet. 2004 Aug;12(8):654-62. doi: 10.1038/sj.ejhg.5201206. Eur J Hum Genet. 2004. PMID: 15138457

2

Predictive testing for Huntington's disease: protocol of the UK Huntington's Prediction Consortium.

Craufurd D, Tyler A. Craufurd D, et al. J Med Genet. 1992 Dec;29(12):915-8. doi: 10.1136/jmg.29.12.915. J Med Genet. 1992. PMID: 1479607 Free PMC article. No abstract available.

3

The uptake and acceptability to patients of cystic fibrosis carrier testing offered in pregnancy by the GP.

Hartley NE, Scotcher D, Harris H, Williamson P, Wallace A, Craufurd D, Harris R. Hartley NE, et al. Among authors: craufurd d. J Med Genet. 1997 Jun;34(6):459-64. doi: 10.1136/jmg.34.6.459. J Med Genet. 1997. PMID: 9192264 Free PMC article.

4

Uptake of genetic testing for cancer predisposition.

Evans DG, Maher ER, Macleod R, Davies DR, Craufurd D. Evans DG, et al. Among authors: craufurd d. J Med Genet. 1997 Sep;34(9):746-8. doi: 10.1136/jmg.34.9.746. J Med Genet. 1997. PMID: 9321761 Free PMC article.

5

Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium.

Harper PS, Lim C, Craufurd D. Harper PS, et al. Among authors: craufurd d. J Med Genet. 2000 Aug;37(8):567-71. doi: 10.1136/jmg.37.8.567. J Med Genet. 2000. PMID: 10922381 Free PMC article.

6

Comparison of genetic services with and without genetic registers: access and attitudes to genetic counselling services among relatives of genetic clinic patients.

Kerzin-Storrar L, Wright C, Williamson PR, Fryer A, Njindou A, Quarrell O, Donnai D, Craufurd D. Kerzin-Storrar L, et al. Among authors: craufurd d. J Med Genet. 2002 Dec;39(12):e85. doi: 10.1136/jmg.39.12.e85. J Med Genet. 2002. PMID: 12471223 Free PMC article.

7

Comparison of proactive and usual approaches to offering predictive testing for BRCA1/2 mutations in unaffected relatives.

Evans DG, Binchy A, Shenton A, Hopwood P, Craufurd D. Evans DG, et al. Among authors: craufurd d. Clin Genet. 2009 Feb;75(2):124-32. doi: 10.1111/j.1399-0004.2008.01146.x. Clin Genet. 2009. PMID: 19215246

8

Discrepancies in reporting the CAG repeat lengths for Huntington's disease.

Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network. Quarrell OW, et al. Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136. Epub 2011 Aug 3. Eur J Hum Genet. 2012. PMID: 21811303 Free PMC article.

9

22 Years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium.

Baig SS, Strong M, Rosser E, Taverner NV, Glew R, Miedzybrodzka Z, Clarke A, Craufurd D; UK Huntington’s Disease Prediction Consortium; Quarrell OW. Baig SS, et al. Among authors: craufurd d. Eur J Hum Genet. 2016 Oct;24(10):1396-402. doi: 10.1038/ejhg.2016.36. Epub 2016 May 11. Eur J Hum Genet. 2016. PMID: 27165004 Free PMC article.

10

Molecular genetics in the National Health Service in Britain.

Harris R, Elles R, Craufurd D, Dodge A, Ivinson A, Hodgkinson K, Mountford R, Schwartz M, Strachan T, Read A. Harris R, et al. Among authors: craufurd d. J Med Genet. 1989 Apr;26(4):219-25. doi: 10.1136/jmg.26.4.219. J Med Genet. 1989. PMID: 2523972 Free PMC article.

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