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.
| Translated title of the contribution | Array-comparative genomic hybridization is a new and promising method for prenatal chromosomal diagnosis. |
|---|---|
| Original language | Danish |
| Journal | Ugeskrift for læger [online] |
| Volume | 176 |
| Issue number | 30 |
| Pages (from-to) | 1379-1382 |
| Number of pages | 4 |
| ISSN | 1603-6824 |
| Publication status | Published - 21 Jul 2014 |
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