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CHROMOSOME ANALYSIS
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Blood – routine Q or G banding. |
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Blood – mosaic, Fragile – X , or high resolution. |
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Amniotic fluid. |
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Chorionic villi. |
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Cancer cytogenetics. |
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Fetal blood sample. |
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Tissue. |
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BIOCHEMISTRY |
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Triple Marker screening [MSAFP , hcc , uE3]. |
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First trimester screening (hcg & PAPP-A). |
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Neonatal screening (Routine). |
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Neonatal screening (Extended). |
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Alpha fetoprotein – Amniotic fluid. |
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Molecular Cytogenetics: |
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Fish technique for |
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Microdeletions , low level mosiacism. |
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Hematologic malignancies. |
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Prenatal diagnosis of trisomies & sex determination. |
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DNA STUDIES |
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For diagnosis and carrier detection of some diseases |
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Duchenne and Beckers muscle dystrophies |
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Spinal muscle atrophy |
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Thalassemia |
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Hemophilia |
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Cystic filorosis |
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DNA studies for paternity determination is all available |
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Reporting
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• All reports are reviewed by certified clinical cytogeneticists and include interpretation and recommendations.
• All abnormal results could be discussed directly with the referring physician by a medical geneticist.
• Reports can be Faxed or E-mailed.
• Reports can be downloaded from our website (very soon ). |
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Immediate fax report and subsequent written reports with karyotype.
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