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Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities
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Grimshaw, G. M., Szczepura, Ala, Hultén, Maj A., MacDonald, F. and Nevin, N. C. (2003) Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities. Health Technology Assessment, Vol.7 (No.10). ISSN 1366-5278
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| Item Type: | Journal Item |
|---|---|
| Subjects: | R Medicine > RJ Pediatrics |
| Divisions: | Faculty of Medicine > Warwick Medical School |
| Library of Congress Subject Headings (LCSH): | Prenatal diagnosis, Chromosome abnormalities |
| Journal or Publication Title: | Health Technology Assessment |
| Publisher: | Core Research |
| ISSN: | 1366-5278 |
| Date: | 2003 |
| Volume: | Vol.7 |
| Number: | No.10 |
| Status: | Not Peer Reviewed |
| Access rights to Published version: | Open Access |
| References: | Cochrane AL, Holland WW. Validation of screening procedures. Br Med Bull 1971;27:3. Department of Health. Screening of pregnant women for hepatitis B and immunisation of babies at risk. Department of Health; 1998. (Health Service Circular: HSC 1998/127). Gray JAM. Dimensions and definitions of screening. Milton Keynes: NHS Executive Anglia and Oxford, Research and Development Directorate; 1996. Holland WW, Stewart S. Screening in healthcare. The Nuffield Provincial Hospitals Trust; 1990. Sackett DL, Holland WW. Controversy in the detection of disease. Lancet 1975;2:357–9.# Wald NJ (editor). Antenatal and neonatal screening. Oxford: Oxford University Press; 1984. Wilson JMG, Jungner G. Principles and practice of screening for disease. Public Health Paper Number 34. Geneva: WHO; 1968. |
| URI: | http://wrap.warwick.ac.uk/id/eprint/276 |
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