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NOONAN SYNDROME AND RELATED DISORDERS , PRENATAL DIAGNOSIS NEXT-GENERATION SEQUENCING (NGS) 17 GENES
| Test Code |
56194 |
|---|---|
| Gene/s |
See all genes  Hide all genes  17 genes |
| Specific Gene |
BRAF, CBL, HRAS, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PTPN11, RAF1, RASA2, RIT1, SHOC2, SOS1, SOS2, SPRED1 |
| Analysis Methods |
Massive sequencing data analysis (NGS) |
| Sample Requirements |
20 mL of amniotic fluid. Chorionic villus is also valid . Necessary clinical and family history. |
| TAT |
30 days |
| Omim G |
– |
| Omim F |
– |
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Do you need more information?
Contact us at
genetics@referencelaboratory.es
Are you a verified customer?
Ordering a test or Service from
us is simple and quick
Check our sample requirements
We have optimized all our processes to accept a wide range of samples, always adapting to each case.