Wolf-Hirschhorn Syndrome FISH Analysis

Related Gene(s): LETM1, MSX1, NSD2

Wolf-Hirschhorn syndrome (chromosome location 4p16.3) FISH (fluorescence in situ hybridization) is offered for diagnosis of individuals with clinical features of Wolf-Hirschhorn syndrome, including intellectual disability, growth retardation, epilepsy, and speech problems. The detection rate of FISH analysis for this disorder is approximately 99%.

Specimen Requirements


  • Amniotic fluid: Minimum total specimen size 15 mL
  • Chorionic villi: Minimum total specimen size 4 mg


  • Whole blood: Minimum 5-10 mL in sodium heparin tube (green top)

Ordering Information


  • Ship at room temperature

Turnaround Time

  • Prenatal: 5-7 days
  • Postnatal: 7-10 days


Prenatal Test Requisition with Natera NIPT
Prenatal Test Requisition with Sequenom NIPT
General Test Requisition