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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
p53-related cancer predisposition (Li-Fraumeni Syndrome) – TP53 sequencing + MLPA
PAI1 4G/5G Polymorphism
Pancreatic Cancer NGS Panel – full sequencing across 22 genes + deletions/duplications
Pancreatic Peptide
Pancreatitis (Hereditary) – PRSS1 hotspot sequencing + deletions/duplications + SPINK1 N34S common mutation
Pan-Ethnic/Jewish Carrier Screening
PAPT and HPV
Paracetamol
Paraganglioma/Pheochromocytoma NGS Panel – full sequencing across 11 genes + deletions/duplications
Paragomius Serology
Parathyroid Antibodies
Parathyroid Hormone (Whole)
Parathyroid Related Peptide
Parvalbumins
Parvovirus Antibodies (IgM)
Parvovirus DNA by PCR
Parvovirus IgG Antibodies
Parvovirus IgG/IgM Abs
Paternity Testing (postnatal and prenatal) – sample required from each person being tested (3 people)
Paul Bunnell (Monospot)
Peach Components
Peanut Components
Pelizaeus-Merzbacher Disease – PLP1 sequencing + deletions/duplications
Pemphigus/Pemphigoid Autoantibodies
Pendred Syndrome – SLC26A4 gene sequencing
Penicillin Antibiotic Panel (BaHRT)
Periodic Fever/Autoinflammation NGS Panel – full sequencing across 36 genes
Perioperative Anaphylaxis Panel (BaHRT)
Pertussis (Whooping Cough) Antibodies
PEth (Phosphatidylethanol)
Pethidine – Urine
Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
Phelan-McDermid Syndrome – karyotype + FISH
Phencyclidine (PCP)
Phenobarbitone
Phenytoin (Epanutin)
Pheochromocytoma/Paraganglioma NGS Panel – full sequencing across 11 genes + deletions/duplications
Phosphate
Phosphate (24 hour Urine)
Phospholipid Antibodies
Pigmentation/Oculocutaneous Albinism/ Hermansky-Pudlak Syndrome NGS Panel – full sequencing across 30 genes
Pituitary Antibodies
Pituitary Function Profile
PLAC Test (Lp-PLA2)
Plasma Viscosity
Plasminogen
Plasminogen Activator Inhibitor – 1
Platelet Aggregation Studies
Pleural Fluid for Culture
Pneumococcal Antibodies – Serotype Specific
Pneumococcal Antibody Screen
Pneumococcal Antigen
Pneumocystis Jiroveci (PCP) Examination
Pneumonia (Atypical) Screen
Polcalcins
POLG-Related Disorders – full POLG sequencing + copy number variant
Polio Virus 1, 2, 3 Antibodies
Polycystic Kidney/NGS Panel – full sequencing across 6 genes
Polycystic Ovary Syndrome Profile
Polycystic Ovary Syndrome SHORT
Pontocerebellar Hypoplasia NGS Panel – full sequencing across 9 genes
Porphyrin (Blood)
Porphyrins (Faeces)
Porphyrins Full Screen (Total: Urine, Stool, Blood)
Porphyrins Screen (Urine)
Postnatal array CGH
Post-Travel Screen 1 (Prior to 6 weeks)
Post-Travel Screen 2 (Prior to 6 weeks)
Potassium
PR-10 Proteins
Prader-Willi Syndrome (Primary Screen) – methylation PCR
Prealbumin
Pregnancy (Serum) [Quantitative]
Pregnancy Test (Urine)
Pregnanetriol (Urine)
Pregnenolone
Prenatal array CGH
Prenatal Diagnosis (BOBs + Culture)
Prenatal Diagnosis for haemoglobinopathies
Pre-Travel Screen (DVT)
Primary Ciliary Dyskinesia (PCD) NGS Panel – full sequencing of 38 genes
Primary Hyperoxaluria Panel – full sequencing across 3 genes + CNV
Primidone (Mysoline)
Procalcitonin
Procollagen 1 Peptide N-Terminal (NTX)
Procollagen III Peptide
Product of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
Product of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
Products of Conception (BOBs + Culture)
Profilins
Progesterone
Proinsulin
Prolactin
Prolactin (Macro)
Propanalol
Propoxyphene
Prostate Cancer NGS Panel – full sequencing across 12 genes + deletions/duplications
Prostate Profile (Total & Free PSA)
Prostate Specific Antigen (Total)*
Prostatic Acid Phosphatase
Protein (Urine)
Protein 14.3.3 (Creutzfeldt–Jakob Disease)
Protein C
Protein C Deficiency – PROC Gene Variant Analysis (Known Genotype)
Protein C Deficiency – PROC Gene Variant Analysis (Unknown Genotype)
Protein Electrophoresis incl. immunoglobin
Protein S Free Ag
Protein Total (Blood)
Protein/Creatinine Ratio (Urine)
Proteinase 3 Ab
Prothrombin Time
Prothrombin Time + Dose
Pseudoachondroplasia (Multiple Epiphyseal Dysplasia) – COMP hotspot sequencing
PTEN-related disorders (including Bannayan-Riley- Ruvalcaba, Cowden & Proteus Syndromes) – sequencing + deletions/duplications
Purkinje Cell Antibody (Hu and Yo)
Pyruvate Kinase (M2-PK)
Pyruvate Kinase (M2-PK)