Genetic Tests
Showing 73–84 of 112 results
-
Morbus Fabry (GLA gene sequencing)
-
MPL გენი (p.W515L/K წერტილოვანი მუტაციები (ექსონ 10)), მეთოდი: პჯრ რეალურ დროში
-
Mucoviscidosis (i.e., cystic fibrosis) – analysis of the 31 most common CFTR gene mutations (as an additional test to neonatal s
-
Myeloproliferative Syndrome (MPS) genetic panel I by RT-PCR:(JAK 2 (p.V617F); CALR exon 9; MPL W515L/K)
-
Myeloproliferative Syndrome (MPS) genetic panel II: JAK 2 (p.V617F); CALR exon 9 and MPL; BCR/ABL (FISH)
-
Myeloproliferative syndrome (MPS) genetic panel: Jak2 p.V617F; Jak2-Exon 12 mutations , MPL, CALR and BCR/ABL-FISH
-
Myeloproliferative syndrome (MPS) genetic panel: Jak2-Exon 14 (p.V617F); Jak2-Exon 12 mutations, MPL, CALR and cKIT (D816V).
-
Myeloproliferative syndrome (MPS) genetic panel: Jak2-Exon 14 (p.V617F); Jak2-Exon 12 mutations.
-
Neonatal screening test (≤49 diseases, including SMA, G6PD deficiency, SCID)
-
Neurofibromatosis / Schwannomatosis (5 genes analyses by NGS)
-
Non Invasive Prenatal Test (NIPT)
-
PAI 1 (Plasminogen-Aktivator-Inhibitor-1) Polymorphismus (4G/5G)