Peripheral Blood Chromosome Analysis (Karyotype Test)

Chromosome disorders form a major category of genetic disease. In a clinical setting, chromosome abnormalities account for a large proportion of patients with dysmorphism congenital malformations, intellectual disability, and infertility or recurrent pregnancy loss, problems of sexual development.

Specimen  requirement - 2 ml of peripheral  blood collected in  heparin (green top) vacutainer tube. 

Reporting time - 21 days

*There will be an additional 20000 AMD added to any newborn trisomy FISH screen.

For further information please contact:
Tel.: (+374 10) 544367
Fax: (+374 10) 544366

Price: 17 000 AMD