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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
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Medical Genetics Test Details

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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

(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
Deletion/Duplication Analysis BCS1L Deletion/Duplication Analysis
Test Code: 3113
Sequence & Deletion/Duplication Analysis BCS1L Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 3114
Sequence Analysis BCS1L Sequence Analysis
Test Code: 3110 		BCS1L Sequence Analysis
Test Code: 3111

This test can only be performed if there is a previously identified familial mutation.
 		BCS1L Prenatal Sequence Analysis (GeneAware)
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.
 BCS1L Sequence Analysis
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.