Genetics - microarray-prenatal, whole genome
| Test Information | |
|---|---|
| Test Name | Genetics - microarray-prenatal, whole genome |
| Lab (Location) | North York General Hospital |
| Category | Chromosomal Anomalies |
| Subcategory | Microarray: Microduplication/deletion Syndrome- Prenatal |
| Gene/Platform/Region List | Genome |
| Test type | Cytogenetic |
| Samples Accepted | DNA, Cultured Cells, Amniocyte, CVS, Tissue |
| Indications Diagnosis | Diagnosis, Prenatal |
| Test Methodology | Microarray |
| Methodology Notes | Microarray |
| Diseases/Conditions | Abnormal prenatal screening, Abnormal ultrasound findings, Multiple congenital anomalies, Advanced maternal age |
| Notes | Before requesting this test, please contact the lab for information regarding eligibility and availability of testing for your patient. |