Background Paper: Summary of WONCA 98 Workshops: Family doctors talk genetics

European Journal of General Practice

Volumn 5, Issue 1, 1999, Pages 33-34

  Oureshi, Nadeem ^a  

^a QUEEN S MEDICAL CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0006273983     PISSN: 13814788     EISSN: 17511402     Source Type: Journal    
DOI: 10.3109/13814789909094250     Document Type: Conference Paper

References (10)

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3. Qureshi N, Raeburn JA. Clinical genetics meets primary care. Br Med J 1993;307:816-7. (Pubitemid 23281743)
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5. Silverman J, Kurtz S. Draper J. Skills for Communicating with Patients. Abingdon, Oxon: Radcliffe Medical Press, 1998.
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7. Brorsson A, Troein M, Lindbladh E, Selander S, Widlund M, Rastam L. My family dies from heart attacks. How hypercholesterolaemic men refer to their family history. Fam Pract 1995;12:433-7. (Pubitemid 26019893)
8. Firth HV, Lindenbaum RH. UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders. J Med Gen 1992;29:20-3.
9. Watson EK, Mayall E, Chappie J, et al. Screening for carriers of cystic fibrosis through primary health care services. Br Med J 1991;303:504-7.
10. Modell M, Wonke B, Anionwu E, et al. A multidisciplinary approach for improving services in primary care: randomised controlled trial of screening for haemoglobin disorders. Br Med J 1998;317:788-91. (Pubitemid 28427236)