CONNEXIN 30 MUTATION DETECTION

174 Ratings

Rs 7,074 Rs 5,400

24 % OFF

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.

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