Medical Genetics Test Details
View Custom Req | Tests in Custom Req: 0
MTRR Related Disorders tests available.
Homocystinuria type cblE | Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism cblE Complementation Type | Methylcobalamin Deficiency cblE Type
(Click the blue dot to view test details. Red dot = current test.)
Diagnostic Testing | Familial Mutation/Variant Analysis | Mutation Testing General Population | Prenatal Diagnosis | Presymptomatic Testing | |
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Deletion/Duplication Analysis |
![]() Test Code: 2568 |
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Sequence & Deletion/Duplication Analysis |
![]() Test Code: 2569 |
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Sequence Analysis |
![]() Test Code: 2565 |
![]() Test Code: 2566 This test can only be performed if there is a previously identified familial mutation. |
![]() Test Code: 2567 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363. |