Molecular services

 

 

 

Molecular and prenatal diagnosis is done for the following genetic diseases :

1. Spinal muscular atrophy (SMA type I, II, III).
2.  β-Thalassemia
3. Cystic fibrosis(CF)
4. Duchenne/ Becker muscular atrophy (DMD/BMD)
   
5. Factor V Leiden
6. MCAD
7. Deafness
8. Sterility due to deletions in AZFa,AZFb, AZFc, AZFd and  DAZ loci 
9. Myotonic dystrophy (DM) 
10.  Friedreich Ataxia
11. Fragile X Syndrome
12. Sex Determination
13. Huntington Disease
14. Celiac Disease
15. HLA typing for Transplantation
16. Monitoring Transplantation by molecular testing for chimeras in bone marrow
17. APOE and PS2  genotyping
18. Ankylosing Spondylitis
19. Parternity

 

Contact us: Tel:(+98 21)88003811-12