Bacterial Culture, Lower Respiratory
Heparin-PF4 Antibody (HIT)
Subtelomeric Region Anomalies, FISH, Amniotic Fluid
Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
DKC1 Gene Mutation Analysis
von Willebrand Disease 2N (Subtype Normandy), Genotyping
CDKN1C Gene Mutation Analysis
Uniparental Disomy, FISH, Amniotic Fluid
Neurofibromatosis Type 1 (NF1) Gene Mutation Analysis
Fine Needle Aspiration Biopsy and Fine Needle Core Biopsy

Protein C, Functional
Medical Test

Access to Protein C, Functional is restricted.

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