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Array-komparativ genomisk hybridisering er en ny og lovende metode til praenatal kromosomundersögelse
Engelsk titel: Array-comparative genomic hybridization is a new and promising method for prenatal chromosomal diagnosis Läs online Författare: Nörgaard, Lone Nikoline ; Ekelund, Charlotte ; Fagerberg, Christina ; Kjaergaard, Susanne ; Lundström, Majken ; Skibsted, Lillian ; Sperling, Lene ; Sundberg, Karin ; Tabor, Ann ; Vogel, Ida ; Petersen, Olav Björn Språk: Dan Antal referenser: 16 Dokumenttyp: Översikt UI-nummer: 14097243

Tidskrift

Ugeskrift for Laeger 2014;176(15)1379-82 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

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.