F
Fabry Disease: GLA Deletion/Duplication Analysis
Fabry Disease: GLA mRNA Analysis
Familial Dysautonomia: IBKAP Recurrent Mutations
Fanconi Anemia Group C: FANCC Recurrent Mutations
FISH - ALK Breakapart - Fresh Tumour
FISH - ALK Breakapart - Paraffin
FISH - BCL6 Breakapart - Fresh Tumour
FISH - BCL6 Breakapart - Paraffin
FISH - Centromere X/SRY - Cultured Fibroblasts
FISH - Centromere X/SRY - Peripheral Blood
FISH - Chromosome 6 - Fresh Tumour
FISH - Chromosome 6 - Paraffin
FISH - Chromosome Enumeration - Buccal Swab
FISH - Chromosome Enumeration - Paraffin Sections
FISH - Chromosome Enumeration - Peripheral Blood
FISH - Chromosome Enumeration - Peripheral Blood
FISH - Cri Du Chat Syndrome - Cultured Fibroblasts
FISH - Cri Du Chat Syndrome - Peripheral Blood
FISH - DDIT3 Breakapart - Fresh Tumour
FISH - DDIT3 Breakapart - Paraffin
FISH - Enumeration Probes for Chromosomes 4, 10, 17
FISH - Enumeration Probes For Chromosomes 5, 7, 8
FISH - ETV6 Breakapart - Fresh Tumour
FISH - ETV6 Breakapart - Paraffin
FISH - EWSR1 Breakapart - Fresh Tumour
FISH - EWSR1 Breakapart - Paraffin
FISH - FOXO1 Breakapart - Fresh Tumour
FISH - FOXO1 Breakapart - Paraffin
FISH - FUS Breakapart - Fresh Tumour
FISH - FUS Breakapart - Paraffin
FISH - IGH/BCL2 - Fresh Tumour
FISH - KAL1 - Cultured Fibroblasts
FISH - KAL1 - Peripheral Blood
FISH - Marker Chromosomes - Cat Eye Syndrome Critical Region - Cultured Fibroblasts
FISH - Marker Chromosomes - Cat Eye Syndrome Critical Region - Peripheral Blood
FISH - Microdeletion/Microduplication 22q11.2 - Cultured Fibroblasts
FISH - Microdeletion/Microduplication 22q11.2 - Peripheral Blood
FISH - Microdeletion 1p (1p36) - Cultured Fibroblasts
FISH - Microdeletion 1p (1p36) - Peripheral Blood
FISH - Miller-Dieker Syndrome - Cultured Fibroblasts
FISH - Miller-Dieker Syndrome - Peripheral Blood
FISH - MYC (8q24) - Fresh Tumour
FISH - MYC Breakapart - Fresh Tumour
FISH - MYC Breakapart - Paraffin
FISH - Paediatric Acute Lymphoblastic Leukemia Panel
FISH - PDGFB Breakapart - Fresh Tumour
FISH - PDGFB Breakapart - Paraffin
FISH - Prader Willi/Angelman Syndrome - Cultured Fibroblasts
FISH - Prader Willi/Angelman Syndrome - Peripheral Blood
FISH - RB1 - Cultured Fibroblasts
FISH - RP11 BAC Clone Microarray Follow Up - Cultured Fibroblasts
FISH - RP11 BAC Clone Microarray Follow Up - Peripheral Blood
FISH - RUNX1 (AML1) and RUNX1T1 (ETO)
FISH - SHOX - Cultured Fibroblasts
FISH - SHOX - Peripheral Blood
FISH - Smith-Magenis Syndrome/Potocki Lupski Syndrome - Cultured Fibroblasts
FISH - Smith-Magenis Syndrome/Potocki-Lupski Syndrome - Peripheral Blood
FISH - Spectral Karyotyping - Bone Marrow Aspirate/Unstimulated Peripheral Blood
FISH - Spectral Karyotyping - Cultured Fibroblasts
FISH - Spectral Karyotyping - Fresh Tumour
FISH - Spectral Karyotyping - Peripheral Blood
FISH - STS - Cultured Fibroblasts
FISH - SYT Breakapart - Fresh Tumour
FISH - SYT Breakapart - Paraffin
FISH - Whole Chromosome Paints - Cultured Fibroblasts
FISH - Whole Chromosome Paints - Peripheral Blood
FISH - Williams Syndrome - Cultured Fibroblasts
FISH - Williams Syndrome - Peripheral Blood
FISH - Wolf-Hirschhorn Syndrome - Cultured Fibroblasts
FISH - Wolf-Hirschhorn Syndrome - Peripheral Blood
FISH - XIST - Cultured Fibroblasts
FISH - XIST - Peripheral Blood
Flow Cytometry Consultation Immunophenotyping
Focal Segmental Glomerulosclerosis Panel: Sequencing
Fragile X E Syndrome: FMR2 Trinucleotide Repeat Analysis
Fragile X Syndrome: FMR1 Trinucleotide Repeat Analysis
Free and Total Carnitine, Plasma/Serum
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