|Values are valid only on day of printing.|
Diagnostic, targeted testing for hemophilia B when a mutation has been identified in a family member
Carrier testing of females in whom the familial F9 genotype is known
Documentation of the specific familial mutation must be provided with the specimen in order to perform this test.
|Test ID||Reporting Name||Available Separately||Always Performed|
|MATCC||Maternal Cell Contamination, B||Yes||No|
Maternal cell contamination testing will be performed for all cord blood specimens. A maternal whole blood sample is required to perform this test.
The following algorithms are available in Special Instructions:
-Hemophilia Carrier Testing Algorithm
-Hemophilia Testing Algorithm
Polymerase Chain Reaction (PCR)/Fluorescent DNA Sequencing
(PCR is utilized pursuant to a license agreement with Roche Molecular Systems, Inc.)