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Rigshospitalet - a part of Copenhagen University Hospital
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Array-komparativ genomisk hybridisering er en ny og lovende metode til prænatal kromosomundersøgelse

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  3. Severe foetal anaemia caused by undetected alloimmunisation in a RhD-positive pregnant woman

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  4. Kongenitte portosystemiske shunter, diagnose og behandling af en multisystemisk sygdom hos børn

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  5. Prenatal detection rate of major congenital heart defects in Copenhagen from 2015 to 2018

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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 contributionArray-comparative genomic hybridization is a new and promising method for prenatal chromosomal diagnosis.
Original languageDanish
JournalUgeskrift for læger [online]
Volume176
Issue number30
Pages (from-to)1379-1382
Number of pages4
ISSN1603-6824
Publication statusPublished - 21 Jul 2014

ID: 44623927