Detection of Chromosomal Abnormalities
If you have a history of pregnancy losses, a malformed foetus or stillbirth or suspect any X-linked disorder in your children, you should perform the test. A special method called Karyotyping is used to detect various chromosomal abnormalities of an individual by using their blood sample. Different types of analyses are included under this technique:

• Peripheral Blood Chromosome Analysis
• Sister chromatid exchange (SCE)
• Chromosome Breakage
• Prenatal Diagnosis
• Solid tissue analysis (conception products, abortus)
• Bone Marrow Cytogenetic Analysis
• Fluorescence In-Situ Hybridisation (FISH) Analysis

We also offer Genetic analyses for the diagnosis of the following conditions. The test options are as follows:  

• Y microdeletions test
• Genetic investigation for sperm aneuploidy using FISH.
• Duchenne/Becker MD
• Ataxia telangiectasia
• Fragile X syndrom
• Thalassemia
• Philadelphia chromosome
• Other tests
• HLA Tissue typing.
• HLA- A, B, C;
• HLA-B27
• HLA-B5
• HLA-DR

STEP 1