Test Name | Test Code | Specimen | Schedule | TAT | Division |
---|---|---|---|---|---|
mdsFiSH - Microdeletion DiGeorge-VCFS (22q) (AF) | CG2034 | 10 ml Amniotic Fluid in Sterile Culture Tube | Daily | 10 days | Cytogenetics |
mdsFISH - Microdeletion DiGeorge-VCFS (22q) (POC) | CG2035 | POC in Sterile Specimen Container (SSC) having Saline+5 drops gentamycin | Daily | 10 days | Cytogenetics |
mdsFiSH - Microdeletion DiGeorge-VCFS (22q) (VB) | CG2036 | 2 ml Fetal/ Cord Blood Sod. Heparin Tube (GCT) | Daily | 10 days | Cytogenetics |
mdsFiSH - Microdeletion Miller Dieker Syndrome (17p13.3) (AF) | CG2037 | mdsFiSH - Microdeletion Miller Dieker Syndrome (17p13.3) [AF] | Daily | 10 days | Cytogenetics |
mdsFiSH - Microdeletion Miller Dieker Syndrome (17p13.3) (VB) | CG2038 | 5 ml Venous Blood Sod. Heparin Tube (GCT) | Daily | 15 days | Cytogenetics |
mdsFiSH - Microdeletion Smith-Magenis (17p11.2) (AF) | CG2039 | 10 ml Amniotic Fluid in Sterile Culture Tube | Daily | 10 days | Cytogenetics |
mdsFiSH - Microdeletion Smith-Magenis (17p11.2) (VB) | CG2040 | 5 ml Venous Blood Sod. Heparin Tube (GCT) | Daily | 15 days | Cytogenetics |
mdsFISH - Microdeletion Williams syndrome (7q11.2) (AF) | CG2041 | 10 ml Amniotic Fluid in Sterile Culture Tube | Daily | 10 days | Cytogenetics |
mdsFISH - Microdeletion Williams syndrome (7q11.2) (VB) | CG2042 | 5 ml Venous Blood Sod. Heparin Tube (GCT) | Daily | 15 days | Cytogenetics |
mdsFISH - Microdeletion Wolf-Hirchhorn Syndrome (4p16 ) (AF) | CG2043 | 10 ml Amniotic Fluid in Sterile Culture Tube | Daily | 10 days | Cytogenetics |
mdsFISH - Microdeletion Wolf-Hirchhorn Syndrome (4p16 ) (VB) | CG2044 | 5 ml Venous Blood Sod. Heparin Tube (GCT) | Daily | 15 days | Cytogenetics |
mdsFiSH-Microdeletion Prader Willi / Angelman Syndrome (15q) (AF) | CG2045 | 10 ml Amniotic Fluid in Sterile Culture Tube | Daily | 10 days | Cytogenetics |
mdsFiSH-Microdeletion Prader Willi / Angelman Syndrome (15q) (POC) | CG2046 | POC in Sterile Specimen Container (SSC) having Saline+5 drops gentamycin | Daily | 10 days | Cytogenetics |
mdsFiSH-Microdeletion Prader Willi / Angelman Syndrome (15q) (VB) | CG2047 | 5 ml Venous Blood Sod. Heparin Tube (GCT) | Daily | 15 days | Cytogenetics |
MPL1 Mutation Analysis (Myeloproliferative Leukemia) | MG3054 | 5 ml Blood or 3 ml Bone marrow in K2/K3 EDTA Tube (LCT) | Daily | 7 days | Molecular Genetics |
MTHFR Two Mutation Test (C677T & A1298C) | MG3055 | 5 ml Blood in K2/K3 EDTA Tube (LCT) | Daily | 7 days | Molecular Genetics |
Myotonic dystrophy (DM) Molecular Analysis | MG3056 | 5ml Blood in K2/K3 EDTA Tube (LCT) | Daily | 15 days | Molecular Genetics |
MITO - Leigh syndrome Target Mutation Analysis | MG3115 | 5ml Blood in K2/K3 EDTA Tube (LCT) | Daily | 3 weeks | Molecular Genetics |
MITO - LHON Target Mutation Analysis (Leb Hered Optic atrophy ) | MG3116 | 5ml Blood in K2/K3 EDTA Tube (LCT) | Daily | 3 weeks | Molecular Genetics |
MITO - MELAS Target Mutation Analysis | MG3117 | 5ml Blood in K2/K3 EDTA Tube (LCT) | Daily | 10 days | Molecular Genetics |