PRADER-WILLI SYNDROME MUTATION DETECTION METHYLATION SPECIFIC PCR
157 Ratings
Rs 11,004 Rs 8,400
24 % OFF
PRADER-WILLI SYNDROME (PWS) AND ANGELMAN SYNDROME (AS) ARE CLINICALLY DISTINCT NEURODEVELOPMENTAL GENETIC DISORDERS THAT MAP TO 15Q11-Q13. THE PRIMARY PHENOTYPES ARE ATTRIBUTABLE TO LOSS OF EXPRESSION OF IMPRINTED GENES WITHIN THIS REGION WHICH CAN ARISE BY MEANS OF A NUMBER OF MECHANISMS. THE MOST SENSITIVE SINGLE APPROACH TO DIAGNOSING BOTH PWS AND AS IS TO STUDY METHYLATION PATTERNS WITHIN 15Q11-Q13.
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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.
METHYLATION SPECIFIC PCR
REPORT ON 15TH DAY EVENING 7PM
DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.
