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
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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
Email: lonenoergaard@dadlnet.dk
Språk: Dan
Antal referenser: 16
Dokumenttyp:
Översikt
UI-nummer: 14097243
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.