NGS
None
| Product | Type of test | Genes |
|---|---|---|
| Angioedema hereditary | Gene NGS | SERPING1 |
| Aortic valve disease | Gene NGS | NOTCH1 |
| Arterial calcification, generalized, of... | Gene NGS | ENPP1 |
| Arterial tortuosity syndrome | Gene NGS | SLC2A10 |
| Blood group, ABO system | Gene NGS | ABO |
| Branchiootorenal syndrome 1 | Gene NGS | EYA1 |
| Brugada syndrome 2 | Gene NGS | GPD1L |
| Brugada syndrome 3 | Gene NGS | CACNA1C |
| Brugada syndrome 4 | Gene NGS | CACNB2 |
| Brugada syndrome 5 | Gene NGS | SCN1B |
| Brugada syndrome 6 | Gene NGS | KCNE3 |
| Brugada syndrome 7 | Gene NGS | SCN3B |
| Brugada syndrome 8 | Gene NGS | HCN4 |
| Cardiomyopathy, dilated, 1V | Gene NGS | PSEN2 |
| Cardiomyopathy, familial restrictive | Gene NGS | TNNI3 |
| Cardiomyopathy, hypertrophic 6 | Gene NGS | PRKAG2 |
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- Cytoarray (Ige, serum)
- Cytoarray 400K Autismo
- Cytoarray CGH 60k
- Cytoarray Parental (180k)
- Cytoarray Parental (60k)
- Cytoarray + SNP
- Cytoarray Plus + SNP ( 400k)
- Cytoarray Plus 180k
- Cytoarray Plus 1M
- Cytoarray Plus 400k
- Cytoarray Prenatal
- Cytoarray Prenatal 60K with Karyotype
- Cytoarray Prenatal - without bioinformatic analysis
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PGS and PGD using NGSPrenatal DiagnosisNGS Carrier Screening PanelRecurrent Miscarriage TestingWhole Exome Sequencing