The cytogenetic section with several years of successful experience, is able to provide chromosomal examination to families with a suspected child with chromosomal defects or to suspected chromosomal abnormalities by amniocentesis sampling or CVS.
The molecular genetic section of this laboratory, with the help of the world's modern facilities, is capable of examining any genetic disease. The successful experience of past years has been indicative of pre-natal diagnosis and having a healthy child.
Genetic tests are usually performed on the order of a physician or a genetic counselor. Genetic testing does not require fasting, and for each type of examination, usually 5 to 8 cc of blood samples are sufficient. For more information, please contact us.
The genetic counseling section of this laboratory, with more than 10 years of successful consultation by experienced physicians and geneticists, is ready to assist families in need of counseling on the history of any inherited disease in the family.
This laboratory by using NGS devices, as the first center with this technology in the north, and using the best bioinformatics software for analyzing genetic data in patients under study, are ready to provide NIPT or Cell Free DNA test, as well as W.E.S.