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Cytogenetic Diagnostics
At the division of Cytogenetics patient material (blood, skin biopsy, chorion villi, amniotic fluid, bone marrow, etc.)
is investigated in order to identify chromosomal aberrations that are suspected to be responsible for the
clinical symptoms observed in a patient. The diagnostic activities are subdivided into three groups:
prenatal, postnatal and tumour cytogenetics, with each group having their own special interests and expertise.
Click on the group of choice to view background information.
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