Our Tests
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- 13q FISH
- 1p36 FISH
- 20q FISH
- 22q11.2 FISH
- 5q FISH
- 6q21 FISH
- 7q FISH
- ALK FISH (lymphoma)
- ALK Screen (lung cancer)
- Alpha Thalassaemia Screen
- Analgesic Pharmacogenetic Screen
- Angelman Syndrome FISH
- Aortopathy panel
- APOE Screen
- Arrhythmogenic right ventricular cardiomyopathy panel
- ATM FISH
- BCL6 FISH
- BCR/ABL1 FISH (lymphoid tumour)
- BCR/ABL1 PCR
- BRAF Screen
- Brugada syndrome panel
- CALR Screen
- CBFB/MYH11 FISH
- CFTR Mutation Panel (Cystic Fibrosis and CBAVD)
- Chronic Lymphocytic Leuk FISH
- Coeliac Disease HLA Typing
- Cri du Chat Syndrome FISH
- CYP2C19 Screen
- CYP2C9 Screen
- CYP2D6
- DAZ Gene (Y Microdeletion)
- Dilated cardiomyopathy panel
- DPYD Screen
- EGFR FISH
- EGFR Screen
- Eosinophilia FISH Panel
- ETV6/RUNX1 FISH
- Ewing Sarcoma FISH
- Factor V Leiden
- FGFR1 FISH
- FMF Screen
- FOXO1 FISH
- Fragile X Syndrome
- FUS/DDIT3 FISH
- Haemochromatosis Type 1
- Harmony Non-Invasive Prenatal Test
- Hereditary Angioedema (I & II)
- Hereditary Angioedema (III)
- HLA Panel Screen (DR and DQ)
- HLA-B1502
- HLA-B27
- HLA-B51
- HLA-B5701
- HLA-B5801
- Hypercholesterolaemia panel
- Hypertriglyceridaemia panel
- Hypertrophic cardiomyopathy panel
- IGH/BCL2 FISH
- IGH/CCND1 FISH
- IGH/MAF FISH
- IGH/MALT1 FISH
- IGH/MYC FISH
- Immigration Relationship Test
- JAK2 Screen
- KAL1 FISH, FGFR1 FISH
- Karyotype (amniocentesis)
- Karyotype (blood)
- Karyotype (CVS)
- Karyotype (leukaemia/lymphoma)
- Karyotype (product of conception)
- Karyotype (tumour)
- KMT2A FISH
- KRAS and NRAS Screen
- Left ventricular non-compaction panel
- Long QTS panel
- Lymphoma Panel
- MDM2 FISH
- Microarray
- Miller-Dieker Syndrome FISH
- MLLT3/KMT2A FISH
- MTHFR Screen
- Multiple Hit Lymphoma FISH
- Multiple Myeloma Panel
- MYC FISH
- MYCN FISH
- Myelodysplastic Syndrome FISH
- Non-Invasive Prenatal Test
- Oligodendroglioma FISH
- PDGFRA/FIP1L1 FISH
- PDGFRB FISH
- Pharmacogenetic Screen
- PML/RARA FISH
- Prader-Willi Syndrome FISH
- Preconception Carrier Screening Panel (CF, SMA and Fragile X)
- Prenatal Paternity
- Prosigna
- Prothrombin Gene
- PTEN FISH
- Pulmonary hypertension panel
- Rapid Interphase FISH
- Rapid Prenatal FISH
- Relationship Testing
- RPN1/MECOM FISH
- RUNX1/RUNX1T1 FISH
- Sex Mismatch FISH
- SHOX FISH
- Smith-Magenis Syndrome FISH
- Sotos Syndrome FISH
- Specimen Matching
- Spinal Muscular Atrophy (SMN1 gene) – Carrier Screening
- Spinal Muscular Atrophy (SMN1 gene) – Diagnostic Testing
- SRY FISH
- SS18 FISH
- TCR/IGH Rearrangements
- Tissue FISH studies
- TP53 FISH
- TPMT Screen
- TRAPS Screen
- Trisomy 12 FISH
- Trisomy 8 FISH
- USP6 FISH
- Vasculopathy panel
- Warfarin Pharmacogenetic Screen
- Williams Syndrome FISH
- Wolf-Hirschhorn Syndrome FISH
- Y Chromosome FISH