Abstract
Array-comparative genomic hybridization (array-CGH) is a very sensitive method for identifying chromosomal imbalances and is now used on a clinical basis for prenatal diagnosis. This article reviews the advantages and disadvantages of the method, the ethical considerations and the current recommendations for prenatal use in Denmark according to a new national guideline from The Danish Society of Foetal Medicine and the Danish Society of Medical Genetics.
Bidragets oversatte titel | Array-comparative genomic hybridization is a new and promising method for prenatal chromosomal diagnosis. |
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Originalsprog | Dansk |
Tidsskrift | Ugeskrift for læger [online] |
Vol/bind | 176 |
Udgave nummer | 30 |
Sider (fra-til) | 1379-1382 |
Antal sider | 4 |
ISSN | 1603-6824 |
Status | Udgivet - 21 jul. 2014 |