Y CHROMOSOME MICRO DELETION (16 MUTATIONS)
Y CHROMOSOME MICRO DELETION (16 MUTATIONS)
3452 tests · Vistacyte Path Labs catalogue
Y CHROMOSOME MICRO DELETION (16 MUTATIONS)
Duchenne/Becker Muscular Dystrophy mutation screening (DMD - 26 exons)
Prenatal DMD mutation screening (26 exons)
SPINAL MUSCULAR ATROPHY (SMN1 GENE: EXON 7 & 8 DELETION MUTATION SCREENING)
Prenatal Spinal Muscular Atrophy (SMN1 Gene: Exon 7 and 8 deletion mutation screening)
SPINO CEREBRAL ATAXIA (SCA - SINGLE FORM)
SPINO CEREBRAL ATAXIA (SCA PANEL - 1,2,3,6,7,10 & 12)
CYSTIC FIBROSIS MUTATION SCREENING (CFTR - del 508 )
CYSTIC FIBROSIS MUTATION SCREENING (CFTR - del 508 G551D/R553X G542X)
HUTINGTON DISEASE (HD MUTATION SCREENING)
HAEMOPHILIA - A COMMON MUTATION SCREENING (FACTOR - VIII, INTRON 22 & INTRON 1 INVERSION ANALYSIS)
FRAGILE - X SYNDROME (FMR1)
JAK2 GENE V617F MUTATION DETECTION
FLT3 (ITD D835Y)
VNTR Chimerism Study
HIV-1 PROVIRAL DNA PCR
TOXOPLASMA QUALITATIVE PCR
RUBELLA QUALITATIVE PCR
CHLAMYDIA TRACHOMATIS PCR (QUALITATIVE)
METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR - 2 VARIANTS C677T A1298C)
FACTOR - V LEIDEN MUTATION SCREENING (F5 - G1691A)
FACTOR II MUTATION SCREENING (F2 - G20,21,0A)
METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) FACTOR-V (F5) FACTOR-II (F2)
WARFARIN THERAPEUTIC RESPONSE PREDICTIVE ASSAY (VKORC1 & CYP2C9)