PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR

  • Test Usage:
    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
  • Report Availability:
    Sample by Sat 11 am; Report 12 days
4 Diagnostic Centers found for PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR in Ahmedabad
  • Shop No.1, Savan Apt, Opp.B-2 Surjit, Naran Chamber Lane, Thakkar Nagar Bapunagar Road, India Colony, Bapu Nagar


    8849210244

    akyagnik09@gmail.com

    Collection Center
  • 286/SOBO Center, South Bopal, Bopal, Ahmedabad, Gujarat


    9723214970

    dp014560@gmail.com

    Collection Center
  • A/7, Basement Of K.B.Complex, Dairy Road, Below Balaji Hospital, Mahesana, Gujarat-384002


    9737182440

    hitech33@gmail.com

    Collection Center
  • 3-Abhikram Complex, Near Home Town Furniture Mall, Opposite Bhaikaka Nagar, Thaltej, Ahmedabad-380059


    079 26859105, 9824065920, 8488081642

    neeteen440u@yahoo.co.in

    Collection Center