USEFUL TO IDENTIFY A SECOND MUTATION IN PATIENTS WHO CARRY A SINGLE CX26 MUTATION AND TO DETERMINE THE GENETIC BASIS FOR HEARING LOSS IN AN AFFECTED INDIVIDUAL.
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4 ML (2 ML MIN.) WHOLE BLOOD IN 1 LAVENDER TOP (EDTA) TUBE. SHIP REFRIGERATED. DO NOT FREEZE. DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.
PCR SEQUENCING
REPORT ON 4TH DAY EVENING 7PM
DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.