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Genetic Labs

Houston, Texas

Genetic Laboratory
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Medical Genetics Test Details

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FISH Analysis - DiGeorge/Velocardiofacial Syndrome Panel (22q and 10p)
10p13-p14 Deletion Syndrome | DiGeorge Syndrome 2 | Velocardiofacial Syndrome 2 | 22q11.2 Deletion Syndrome | Cayler Cardiofacial Syndrome | Conotruncal Anomaly Face Syndrome | DiGeorge Syndrome | Opitz G/BBB Syndrome Autosomal Dominant | Sedlackova Syndrome | Shprintzen Syndrome | Velocardiofacial Syndrome
Test Information: Confirmation of Clinical Diagnosis
Test Details
Test Code: 8440
Test Includes: This dual-probe FISH assay can detect deletions on chromosome 22q11.2 and chromosome 10p13p14.

Special Notes: For initial screening we recommend CMA - HR (#8655). DiGeorge/Velocardiofacial Syndrome Type II (10p) FISH (#8465) and DiGeorge/Velocardiofacial Syndrome Type I (22q) FISH (#8486) are also available.

There is a GeneReviews for 22q11.2 Deletion Syndrome


Technical Information
Methodology: Fluorescent in Situ Hybridization (FISH) Analysis
Sample & Shipping Information
Test Requisition: Cytogenetics
Specimen Type: Blood
Requirements: Draw blood in a Sodium Heparin (green-top) tube(s) and send 3-5 cc (Adults/Children) or 1-2 cc (Infant< 2 years).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Specimen should arrive in the laboratory within 48 hrs of collection. Do not heat or freeze.

Turn Around Time: 14 days
Billing Information
List Price: $830.00 *Institutional discounts may apply, please call.
CPT Codes: 88230x1, 88271x2, 88273x1, 88291x1, 88280x1


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