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PRADER-WILLI (PW) SYNDROME (MS-MLPA)

PWS is a contiguous gene syndrome due to abnormal DNA methylation within the Prader-Willi critical region (PWCR) at 15q11.2-q13. MS-MLPA is a cost-effective, accurate, and efficient molecular diagnostic tool for PWS.

Whole Blood Sample (EDTA), 3ml
4 - 6 Weeks

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