P | Health Services Laboratories

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Tests: P

Test codes, sample requirements and turnaround times for our most requested tests.

Please use the search box below to filter this list

Test name
P. jirovecii PCR (BAL, Sputum)
p16
p53-related cancer predisposition (Li-Fraumeni Syndrome) – TP53 sequencing + MLPA
PAI1 4G/5G Polymorphism
Pancreatic Cancer NGS Panel – full gene sequencing + deletions/duplications
Pancreatic Islet Cell Antibodies
PAPP A
Paracetamol (Acetaminophen)
Paraganglioma/Pheochromocytoma NGS Panel – full gene sequencing + deletions/duplications
Parathyroid Antibodies
Parathyroid Hormone (PTH)
Parvovirus Antibodies (IgM)
Parvovirus IgG Antibodies
Parvovirus Quantitative DNA by PCR
Paternity Testing (postnatal and prenatal) – sample required from each person being tested (3 people)
Paul Bunnell (Monospot)
PD-L1 (22C3)
PD-L1 (28-8)
PD-L1 (SP142)
PDGRF Antibodies
Pelizaeus-Merzbacher Disease – PLP1 sequencing + deletions/duplications
Pemphigus/Pemphigoid Autoantibodies
Pendred Syndrome – SLC26A4 gene sequencing
Perforin
Periodic Fever/Autoinflammation NGS Panel – full gene sequencing
Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
Phagocytosis Assay
Phelan-McDermid Syndrome – karyotype + FISH
Phenytoin
Pheochromocytoma/Paraganglioma NGS Panel – full gene sequencing + deletions/duplications
Phosphate
Phosphatidylserine Antibodies
Phospholipase A2 Receptor
Pigmentation/Oculocutaneous Albinism/Hermansky-Pudlak Syndrome NGS Panel – full gene sequencing
Pituitary Antibodies
PL-12 Antibodies
PL-7 Antibodies
Plasma Metanephrines (normetanephrine, metanephrine, 3-methoxytyramine)
Plasma Viscosity
Platelet Aggregation Studies
Platelet Antibodies
Platelet function assay (PFA-100 assay)
PM-Scl100 Antibodies
PM-Scl75 Antibodies
PML Antibodies
Pneumococcal Antibodies – Serotype Specific
Pneumococcal Antibody (PCP)
Pneumococcal Urinary Antigen
PNH
PNP (Nucleotide Metabolism)
POLG-Related Disorders – full POLG sequencing + copy number variant
Polio Virus 1, 2, 3 Antibodies
Polycystic Kidney/NGS Panel – full gene sequencing
Pontocerebellar Hypoplasia NGS Panel – full gene sequencing
Postnatal array CGH
Potassium
Prader-Willi Syndrome (Primary Screen) – methylation PCR
Pre-Travel Screen (DVT)
Prenatal array CGH
Prenatal Diagnosis (BOBs + Culture)
Prenatal Diagnosis for haemoglobinopathies
PRF1 (perforin) gene and MUNC 13-4 mutation analysis
Primary Ciliary Dyskinesia (PCD) NGS Panel – full gene sequencing
Primary Hyperoxaluria metabolites (glycolate, glycerate, dihydroxyglutarate)
Primary Hyperoxaluria Panel – full gene sequencing + CNV
Procalcitonin
Product of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
Product of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
Progesterone
Prolactin
Proliferation Assay
Prostate Cancer NGS Panel – full gene sequencing + deletions/duplications
Prostatitis Screening Panel
Protein C
Protein C Deficiency – PROC Gene Variant Analysis (Known Genotype)
Protein C Deficiency – PROC Gene Variant Analysis (Unknown Genotype)
Protein Electrophoresis
Protein S Free Ag
Proteinase 3 Antibodies
Prothrombin Time + Dose
Prothrombin Time
PTEN-related disorders (including Bannayan-Riley-Ruvalcaba, Cowden & Proteus Syndromes) – sequencing + deletions/duplications
Purkinje Cell Antibodies (Hu and Yo)
PVL toxin gene PCR
Pyruvate Kinase