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FRAGILE X SYNDROME , MOLECULAR STUDY (SCREENING + MEDIUM RANGE EXPANSION) GENE FMR1 PCR PRENATAL DIAGNOSIS
| Test Code |
15431 |
|---|---|
| Gene/s |
See all genes  Hide all genes  – |
| Analysis Methods |
Capillary electrophoresis fragment length analysis |
| Sample Requirements |
20 mL amniotic fluid or Chorionic villus sampling. Please, indicate the weeks of pregnancy. 5 mL blood (EDTA)from mother. It´s necessary to send us the clinical and family history. |
| TAT |
21 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.