CGG triplet study in FMR1 (Triplet Expansion)

Delivery time

1-2 weeks

Sample

Blood

139,15€

The study of CGG triplets in the FMR1 gene allows the identification of abnormal expansions that can cause Fragile X syndrome or be associated with premature ovarian insufficiency. It evaluates the number of CGG repeats, differentiating between normal alleles, premutations, and full mutations.

Other tests

Trisomy 11 (Blood. Biopsy tissue)

166,98€

Trisomy 11 (Blood. Biopsy tissue. Bone marrow)