Welcome to the Division of Cytogenetics
A team of experienced geneticists in the division specializing in chromosomes utilizes advanced technology to provide a wide range of cytogenetic services to individuals and families. These services are centered on the examination of chromosomes, which determine our genetic makeup as carriers of genes.
- Karyotyping:
A method that allows us to visualize and analyze the structure and number of chromosomes in a cell. This is useful for identifying genetic disorders, such as Down syndrome, as well as for determining the cause of certain birth defects and infertility issues.
- Chromosome Breakage Studies:
A method that evaluates the ability of cells to repair broken chromosomes, which can be a sign of genetic disorders, such as Fanconi anemia or Bloom syndrome.
- Fragile X Studies:
A test that evaluates the presence of a genetic mutation that can cause intellectual disability and other health problems
- Mutagen Induced Chromosome Sensitivity Studies:
A method that evaluates the ability of cells to repair DNA damage, which can be a sign of genetic susceptibility to certain cancers or other health problems.
- Cytokinesis Block Micronuclei Assay:
A method that quantifies the extent of DNA damage in cells, which can be a sign of exposure to environmental toxins, such as radiation or chemical pollutants.
Genetika, dedicated to providing clients with the highest quality genetic testing and counseling services, operates the Cytogenetics Division. This division is equipped with state-of-the-art technology and is staffed by experienced and knowledgeable professionals who are committed to helping clients understand their genetic results and make informed decisions about their health and well-being.