FRAGILE X (FMR1) MUTATION SCREEN

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Rs 19,240 Rs 14,800

23 % OFF

MUTATIONS IN THE FMR1 GENE CAUSE FRAGILE X SYNDROME. FRAGILE X SYNDROME IS A GENETIC CONDITION THAT CAUSES A RANGE OF DEVELOPMENTAL PROBLEMS INCLUDING LEARNING DISABILITIES AND COGNITIVE IMPAIRMENT. THIS TEST IS USED TO DETERMINE THE NUMBER OF TIME THE CGG TRIPLET IS REPEATED TO DIAGNOSE FRAGILE X SYNDROME.

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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.

TP-PCR, FRAGMENT ANALYSIS

REPORT ON 15TH DAY EVENING 7PM

DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.

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