FISH - Prader Willi Syndrome SNRPN

  • Test Usage:
    Most cases (99%) are caused by absence of a paternal contribution to the imprinted region on chromosome 15q11-q13; approximately 70% of these are due to a large -5-7 Mb deletion.
  • Report Availability:
    Sample Daily by 4 pm; Report 7 Days.
  • Sample Report:
13 Diagnostic Centers found for FISH - Prader Willi Syndrome SNRPN in Bijnor