The genetic testing of children. Working Party of the Clinical Genetics Society (UK)
Open Access
- 1 October 1994
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 31 (10) , 785-797
- https://doi.org/10.1136/jmg.31.10.785
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Adoption, genetic disease, and DNA.Archives of Disease in Childhood, 1993
- Presymptomatic testing for Huntington disease: Is there a duty to test those under the age of eighteen years?American Journal of Medical Genetics, 1993
- Presymptomatic Testing for Huntington's Disease in Wales 1987–90The British Journal of Psychiatry, 1992
- Predictive testing for Huntington disease in Canada: Adverse effects and unexpected results in those receiving a decreased riskAmerican Journal of Medical Genetics, 1992
- Screening for carriers of cystic fibrosis through primary health care services.BMJ, 1991
- Should we test children for "adult" genetic diseases?The Lancet, 1990
- Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986.Journal of Medical Genetics, 1989
- Psychological Consequences of Neonatal Screening for α1‐Antitrypsin DeficiencyActa Paediatrica, 1985
- A private view of heterozygosity: Eight‐year follow‐up study on carriers of the Tay‐Sachs gene detected by high school screening in montrealAmerican Journal of Medical Genetics, 1984
- A genetic register for Huntington's chorea in South Wales.Journal of Medical Genetics, 1982