Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Edwards P. J., Hall D. M. Screening, ethics, and the law. BMJ. 1992 Aug 1;305(6848):267–268. doi: 10.1136/bmj.305.6848.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Firth M., Gardner-Medwin D., Hosking G., Wilkinson E. Interviews with parents of boys suffering from Duchenne muscular dystrophy. Dev Med Child Neurol. 1983 Aug;25(4):466–471. doi: 10.1111/j.1469-8749.1983.tb13791.x. [DOI] [PubMed] [Google Scholar]
- Harper Peter. Genetics and public health. BMJ. 1992 Mar 14;304(6828):721–721. doi: 10.1136/bmj.304.6828.721. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith R. A., Williams D. K., Sibert J. R., Harper P. S. Attitudes of mothers to neonatal screening for Duchenne muscular dystrophy. BMJ. 1990 Apr 28;300(6732):1112–1112. doi: 10.1136/bmj.300.6732.1112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wald N. J., Kennard A., Densem J. W., Cuckle H. S., Chard T., Butler L. Antenatal maternal serum screening for Down's syndrome: results of a demonstration project. BMJ. 1992 Aug 15;305(6850):391–394. doi: 10.1136/bmj.305.6850.391. [DOI] [PMC free article] [PubMed] [Google Scholar]