New molecular cytogenetic techniques
The department is engaged in the development of new molecular cytogenetic techniques (array-CGH among others) and investigation of their clinical usefulness. The department was the first in Scandinavia to offer prenatal array for foetuses with malformation as a first tier analyses. The detection rate is currently 10%. Follow-up results on usual screening parameters as well as rates of TOP, rate of miscarriage, birth and diagnoses will follow.
Contacts:
Ida Vogel or Else Marie Vestergard