Medical Genetics Test Details
View Custom Req | Tests in Custom Req: 0
BCS1L - Related Disorders tests available.
Cytochrome-Related Disease of Muscle and Nervous System | Tubulopathy Encephalopathy and Liver Failure due to Complex III Deficiency | Gracile Syndrome | Leigh Disease | Leigh Syndrome Due to Cytochrome c Oxidase Deficiency | Leigh Syndrome (nuclear DNA mutation) | Mitochondrial Respiratory Chain Complex III Deficiency BCS1L-Related | BJS | Bjornstad Syndrome
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Diagnostic Testing | Familial Mutation/Variant Analysis | Mutation Testing General Population | Prenatal Diagnosis | Presymptomatic Testing | |
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Deletion/Duplication Analysis |
![]() Test Code: 3113 |
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Sequence & Deletion/Duplication Analysis |
![]() Test Code: 3114 |
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Sequence Analysis |
![]() Test Code: 3110 |
![]() Test Code: 3111 This test can only be performed if there is a previously identified familial mutation. |
![]() Test Code: 60197 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. ![]() Test Code: 3112 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. |