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Product | Type of test | Genes |
---|---|---|
Neutropenia, severe congenital 3,... | Gene NGS | HAX1 |
Obesity, morbid, due to leptin deficiency | Gene NGS | LEP |
Paroxysmal nocturnal hemoglobinuria | Gene NGS | PIGA |
Phenylketonuria | Gene NGS | PAH |
Platelet disorder, familial, with... | Gene NGS | RUNX1 |
Prenatal point mutation test | Gene NGS | |
Prenatal Supplement | False | |
Rendu-Osler-Weber syndrome | Gene NGS | ACVRL1 |
Rendu-Osler-Weber syndrome | Gene NGS | ENG |
Rothmund-Thomson syndrome | Gene NGS | RECQL4 |
Telangiectasia, hereditary hemorrhagic,... | Gene NGS | ACVRL1 |
Trichohepatoenteric syndrome 1 | Gene NGS | TTC37 |
Tumoral calcinosis | Gene NGS | GALNT3 |
Tumoral calcinosis | Gene NGS | FGF23 |
Tumoral calcinosis | Gene NGS | KL |