E-Tender For Rate Contract For Medical Laboratory Blood Testing Outsource Service (Part-1) For U N Mehta Institute Of Cardiology And Research Centre (Affiliated To B. J. Medical College & Nabh Accredited) Ahmedabad, Gujarat, India.- Nipt,1 25 Dihydroxy Vitamin D,13, 18, 21 Fish Panel,13, 18, 21, X, Y Fish Panel,17-Oh (Hydroxy) Progesterone,18S Sequencing & Analysis On Illumina Platforms (Sample-1),1P/19Q Deletion,20Q Deletion,24 Hour Total Porphyrins In Urine,24 Hour Urine 17 Ketosteroids,24 Hour Urine 5-Hiaa,24 Hour Urine Albumin,24 Hour Urine Calcium,24 Hour Urine Catecholamines,24 Hour Urine Chloride (Cl-),24 Hour Urine Citrate,24 Hour Urine Copper,24 Hour Urine Cortisol,24 Hour Urine Creatinine,24 Hour Urine Creatinine Clearance Test,24 Hour Urine Magnesium,24 Hour Urine Metanephrine,24 Hour Urine Microalbumin,24 Hour Urine Oxalate,24 Hour Urine Phosphorus,24 Hour Urine Porphobilinogen,24 Hour Urine Potassium(K+),24 Hour Urine Protein,24 Hour Urine Sodium (Na+),24 Hour Urine Urea,24 Hour Urine Urea Nitrogen,24 Hour Urine Uric Acid,24 Hour Urine Vma,24 Hours Diagnostic Panel (Metabolic Study),24 Hours Urine For Protein Electrophoresis,24 Hours Urine Metabolic Stone Screen Test,24 Hours Urine Zinc,3-Methylcrotonyl-Coa Carboxylase Panel - Mccc1, Mccc2,47, Xyy Syndrome,5-Hiaa Urine,5Q Deletion,7Q Deletion,Abcd1 Gene Test,Abpa Panel,Ace (Angiotensin Converting Enzyme) Level,Ace Level Csf,Acetone,Acetylcholine Receptor Antibody (Achr),Achondroplasia (Targeted) - Fgfr3,Acid Phosphatase,Acth Edta Plasma,Activated Protein C Resistance (Apcr),Active B12 Level,Acute Leukemia Reflex Panel,Adenosine Deaminase (Ada),Adh-Anti Diuretic Hormone,Adrenaline (Epinephrine) Plasma,Adrenocorticotropic Hormone (Acth),Adrenoleukodystrophy (Ald),Afb Blood Culture By Bact/Alert 3D,Afb Bone Marrow Culture By Bact/Alert 3D,Afb By Fluorescent Stain,Afb Culture By Bactalert/Bactec (Mgit) Method,Afb Culture By Conventional Method,Afb Fluid,Afb For Three Days,Afb Sensitivity - Single Drug By Bactec Mgit,Afb Sensitivity 13 Drugs,Afb Sensitivity 1St Line Drugs Sirep By Bactec,Afb Sensitivity 1St Line Drugs Sirep,Afb Sensitivity 2Nd Line Drugs By Bactec,Afb Sensitivity 2Nd Line Drugs,Afb Sensitivity By Conventional Method (Single Drug),Afb Sensitivity For Mott,Afb Sensitivity10 (1St And 2Nd Line) Drug Sensitivity By Bactalert/Bactec Mgit,Afb Sensitivity10 (1St And 2Nd Line) Drug Sensitivity By Bactec Mgit,Afb-Mtb Antibiogram-Add Drugs-4Nos. Macc,Afp Fluid,Afp - Mom,Afp (Alpha Feto Protein),Agammaglobulinemia, X-Linked 1 (Xla),Alagille Syndrome 1 (Algs1 ),Alagille Syndrome Panel - Jag1, Notch2,Albert Stain,Albumin,Albumin Creatinine Ratio Urine,Albumin Fluid,Alcohol Level,Aldolase,Aldosterone Level,Aldosterone/Renin Activity Ratio,Alk 1 (Ihc Marker),Alk-1 Mutation,Alkaline Phosphatase,Alkaptonuria Urine Qualitative,All Comprehensive Panel 1,All Fish And Karyotyping Panel,All Fish Panel,All Multiplex Panel - 6 Fusions [T(9;22) T(12;21) T(1;19) T(4;11) T(9;11) T(11;19),All Multiplex Panel (T(9;22) T(12;21) T(1;19) T(4;11),All Panel C - Karyotyping Fish Mll Pcr T(12;21) Pcr T(9;22) Pcr T(1;19),All Panel A- Fish T(12;21) Fish T(9;22) Fish Mll Gene Rearrangement Fish T(1;19),All Panel B- Fish Tel-Aml T(12;21) Fish Bcr-Abl T(9;22) Fish Mll T(1;19),All Positive Panel,Allergen-Amoxicillin (Antibiotic),Allergen-Ampicillin (Antibiotic),Allergen-Cephalosporin (Antibiotic),Allergen-Penicilloyl G (Antibiotic),Allergen-Penicilloyl V (Antibiotic),Allergen-Sulpha (Antibiotic),Allergy - Microarray (300 Allergens ),Allergy Milk,Allergy Test - Drugs,Allergy Test - Food Nonveg,Allergy Test - Food Veg,Allergy Test - Pollens + Contacts,Allergy Test - Veg + Pollens + Contacts,Allergy Test - Veg + Pollens + Contacts + Drugs,Allergy Test - Veg + Pollens + Contacts + Drugs + Nonveg,Allergy Test - Veg + Pollens + Contacts + Nonveg,Allergy Test - Inhalant,Alpha Thalassemia Deletion/ Duplication Analysis By Mlpa,Alpha Thalassemia X-Linked Intellectual Disability Test - Atrx,Alpha Thalassemia/Mental Retardation Syndrome,Alpha-1 Antitrypsin,Alport Syndrome, X-Linked (Ats),Alternaria Alternate - Specific Igg,Alternating Hemiplegia Of Childhood Panel (Upto 5 Genes),Aluminium Level Fluid,Aluminium Level Serum,Alzheimer Disease 1, Familial (Ad1),Amebiasis ( Entamoeba Histolytica) Antibodies-Igg,Amino Acid Quantitative Plasma,Amino Acid Urine,Aml Comprehensive Panel 1,Aml Fish And Karyotyping Panel,Aml Fish Panel,Aml Gene Panel - Basic (Flt3 Npm1 Cebpa),Aml Multiplex Advance (Bcr-Abl Pml-Rara Aml-Eto Inv 16 Npm1 Flt3 Cebpa),Aml Neo Panel -Fish T(8;21) Fish Inv(16) Pcr Npm-1/Cebpa/ Flt -3 Mutation,Aml Panel- Karyotyping Fish Mll Fish T(8;21) Fish T(15;17) Fish Inv(16),Aml Panel- Fish Mll Fish T(8;21) Fish T(15;17) Fish Inv(16),Aml Panel -(Pcr Npm1 Flt3 Dnmt3a Cebpa Idh 1&2),Aml Positive Panel,Aml Prognostic Panel (Aml-Eto/Inv.-16/Pml-Rara/Flt-3),Ammonia,Amoebiasis Antibody-Igg,Amylase,Amylase - Body Fluid,Amylase Urine,Amyotrophic Lateral Sclerosis Panel (Upto 19 Genes),Ana (Elisa),Ana (Ifa),Ana By Clia,Ana Profile (Blot) 25 Parameters,Anca (Ifa),Anca-C (Pr3),Anca-P (Mpo),Anderson-Tawil Syndrome - Kcnj2,Androgen Insensitivity Panel - Ar, Srd5a2, Nr0b1, Nr5a1, Sry,Androgen Insensitivity Syndrome (Ais),Androstenedione,Aneuploidy By Qf-Pcr (With Mcc),Angelman Syndrome (As ),Anion Gap,Aniridia (An),Aniridia Test - Pax6,Anti - Hbs,Anti Cardiolipin Antibody (Igg & Igm),Anti Cardiolipin Antibody Iga,Anti Cardiolipin Antibody Igg,Anti Cardiolipin Antibody Igm,Anti Ccp,Anti Complement Factor H,Anti D Titre,Anti Dnase,Anti Dnase B,Anti Ds Dna (By Ifa),Anti Ds Dna (Elisa),Anti Gad Antibodies (For Type I Diabetes),Anti Gad65 Test Clia,Anti Gbm Antibody (Glomerular Basement Membrane),Anti Hav Igg,Anti Hav Igm,Anti Hav Total,Anti Hbc Igm,Anti Hbcab Igm,Anti Hbcab Total,Anti Hbe Antibodies,Anti Hbs,Anti Hcv By Eclia/Cmia,Anti Hcv By Elisa,Anti Hcv Igm,Anti Hev Igg,Anti Hev Igm,Anti Insulin Antibody,Anti Islet Cell Antibodies,Anti Mag Ab,Anti Mitochondrial Antibody (Ama) By Elisa,Anti Mitochondrial Antibody By Ifa,Anti Mullerian Hormone (Amh),Anti Musk Antibody,Anti Nmo Antibody, Csf,Anti Nmo Antibody, Serum,Anti Parietal Cell Antibody,Anti Phospholipid Antibody Iga,Anti Phospholipid Antibody Igg,Anti Phospholipid Antibody Igm,Anti Phospholipid Igg & Igm,Anti Phospholitic Syndrom Panel,Anti Platelet Factor4(Pf4) Antibody,Anti Smooth Muscle Antibody (Asma),Anti Sperm Ab Serum,Anti Synthetase Antibody Profile,Anti Tg (Anti Thyroglobulin) Antibody,Anti Thrombin Iii,Anti Thyroglobulin Antibody (Atg),Anti Thyroid Antibody (Anti Thyroglobulin Antibody & Anti Tpo),Anti Tpo (Anti Microsomal) Antibody,Anti Treponemal Antibody,Anti Tubercular 3Drugs Panel By Hplc,Anti Vgkc; Csf,Anti Vgkc; Serum,Anti-Centromere(Cenp),Antifungal Sensitivity,Antihistone,Antistreptolysin-O (Aso),Antithrombin Iii Deficiency Test Serpinc1,Aortopathy Comprehensive Panel - 22 Genes,Apc Gene Mutation Analysis On Blocks,Apolipoprotein A1,Apolipoprotein B,Apolipoprotein (A1 & B),Aptt,Aquaporin-4 Antibodies (Nmo-Igg) Csf,Aquaporin-4 Antibodies (Nmo-Igg) Serum,Arsenic Level,Arsenic Level In Liver Biopsy,Arse-Related Chondrodysplasia Punctata Test - Arse,Arterial Blood Gas Analysis (Abg),Asca Iga,Asca Igg,Ascitic Fluid Analysis,Asma By Ifa,Asperger Syndrome,X-Linked, Susceptibility To, 1 (Aspgx1),Aspergillosis Igg,Aspergillosis Igm,Aspergillus (Galactomannan Ag) Serum,Aspergillus (Galactomannan Ag) Bal,Aspergillus Specific Ige,Aspergillus. Fumigatus - Specific Igg,Asphyxiating Thoracic Dystrophy Panel - Dync2h1, Ift80, Ttc21b,Ataxia-Telangiectasia Test - Atm,Á-Athalassemia (Additional Variants) (Single),Á-Thalassemia (Targeted) - 17 Genetic Variants; With Maternal Cell Contamination Analysis,Á-Thalassemia (Targeted) - 17 Genetic Variants,Atp7a-Related Disorders,Atypical Mycobacteria Species Identification,Autism Panel,Auto Hemolysis Test,Autoimmune Encephalitis Panel Csf,Autoimmune Encephalitis Panel Serum,Autoimmune Hepatic Profile,Automated Semen Analysis,Autophagic Vacuolar Myopathy Panel (3 Genes),Avidity Test Rub Igg,Avidity Test Toxo Igg,Avidity Test Cmv Igg,Axenfeld-Rieger Panel - Foxc1, Pitx2, Pax6,Axenfeld-Rieger Syndrome Panel,Bal (Broncho Alveolar Lavage) Analysis,Bal For Cd4/Cd8 Ratio,Bannayan-Riley-Ruvalcaba Syndrome (Brrs),Bap1 Hereditary Cancer Predisposition Syndrome Test - Bap1,Baraitser-Winter Cerebrofrontofacial Syndrome Panel,Bardet-Biedl Syndrome Panel- 15 Genes,Barth Syndrome - Taz,Bartter Syndrome, Antenatal, Type 2,Basal Cell Nevus Syndrome (Bcns),Basal Cell Nevus Syndrome Panel-Ptch1, Sufu, Ptch2,Basal Ganglion Antibody,Bcr-Abl Qualitative By Real- Time Pcr,Bcr-Abl Quantification (Major And Minor) By Real-Time Pcr,Bcr-Abl Quantification (Major) By Real-Time Pcr,Bcr-Abl Quantification (Minor) By Real-Time Pcr,Beckwith-Wiedemann Syndrome (Bws),Bence Jones Protein,Benzodiazapine,Beta 2 Glycoprotein Igg & Igm,Beta 2 Glycoprotein Iga,Beta 2 Glycoprotein Igg,Beta 2 Glycoprotein Igg Igm & Iga,Beta 2 Glycoprotein Igm,Beta 2 Microglobulin,Beta 2 Microglobulin-Urine,Beta Carotene Level,Beta Crosslaps,Beta D Glucan Level Fungitell,Beta Glucosidase Enzyme Assay,Beta Hcg,Beta Thalassemia Deletion/ Duplication Analysis By Mlpa,Beta-Hcg Fluid,Beta-Trace Protein(Btp) Csf Leakage In Body Fluid,Bethesda Assay (Quantitative Factor Inhibitor),Bicarbonate (Hco3),Bile Acid,Bilirubin,Biofire By Multiplex Pcr,Biofire Csf Panel,Biofire Gastro Intestinal (Gi)Panel,Biofire Pneumonia Plus Panel,Biofire Respiratory Panel,Biopsy Endomyocardial (Post Transplant) With C4d And Cd68,Biopsy Large ( ≫ 10 Blocks),Biopsy Medium (4-10 Blocks),Biopsy Small ( 1-3 Blocks),Biotindase Activity,Biotinidase Deficiency Test - Btd (Targeted),Birt-Hogg Dube Syndrome - Flcn,Bkv Qualitative Pcr,Bleeding Time,Blepharophimosis, Ptosis, And Epicanthus Inversus (Bpes),Blood Gas Analysis,Blood Gas Analysis With Electrolyte,Blood Gas With Lectate,Blood Group,Bloom Syndrome - Blm,Bm Aspiration For Stem Cell Collection,Bm Iron Stain,Bnp(B-Type Natriuretic Peptide),Bone Marrow (Bm) Biopsy,Bone Marrow (Bm) Iron Stain,Bone Marrow (Bm) Reporting,Bone Marrow Failure Syndromes Panel - 39 Genes,Borjeson-Forssman-Lehmann Syndrome (Bfls),Borrelia Burgdorferi Igm & Igg,Bp 180 (Bullous Pemphigoid 180 Vesiculobullous Disorders),Bp 230 (Bullous Pemphigoid 230 Vesiculobullous Disorders),Brachydactyly, Type C (Bdc),Brachydacytly-Mental Retardation Syndrome (Bdmr),Branchio-Otorenal Spectrum Disorders Panel - Eya1, Six1, Sall1,Branchiootorenal Syndrome 1 (Bor1),Brca 1 & 2 Deletions/Duplications By Mlpa,Brca1 And Brca 2,Brca1 And Brca2 By Mlpa,Breast And Gynecological Cancers Panel - 35 Genes,Breast Cancer Panel - 26 Genes,Brucella Culture,Brucella Igg,Brucella Igm,Brucellosis Titre,Brugada Syndrome Panel - 20 Genes,Btp (Beta Trace Protein) Test,Bun,Bun/Creatinine Ratio,Buschke-Ollendorff Syndrome (Bos),C Diptheria,C1 Esterase Inhibitor,C1q Complement,C3,C4,Ca 125,Ca 125 Fluid,Ca 15-3,Ca 19-9,Ca 19-9 Fluid,Ca 72.4,Cadmium,Cadmium Level,Calcitonin,Calcium,Calcium 24 Hour Urine,Calcium Creatinine Ratio Urine,Calcium Urine (Random),Calprotectin Stool,Calr Mutation Detection,Campomelic Dysplasia (Cmpd),Campomelic Dysplasia Test - Sox9,Canassist Breast,Canavan Disease Test - Aspa,Cancer Karyotyping,Candida Sensitivity Manual,Capillary Malformation- Arteriovenous Malformation Syndrome Test - Rasa1,Carbamezapine,Carba-R,Cardio-Facio-Cutaneous Syndrome Panel- Braf, Kras, Map2k1, Map2k2, Shoc2, Sos1,Cardiomyopathy And Skeletal Muscle Disease Panel (Upto 158 Genes),Cardiomyopathy Panel,Cardiomyopathy, Dilated, 1J (Cmd1j),Carney Complex Test - Prkar1a,Carpenter Syndrome Panel -Megf8, Rab23,Casr-Related Conditions Test,Cat Eye Syndrome (Ces) ( Genetic Study),Cat Eye Syndrome (Ces) (Fish),Catecholaminergic Polymorphic Ventricular Tachycardia (Cpvt) Panel - Ank2, Calm1, Calm2, Calm3, Casq2, Kcnj2, Ryr2, Trdn,Catecholamines,Catecholamines 24 Hour Urine,Cbc,Cbc - Esr,Cbc-Ps,Cd 19 Count,Cd 20 Count,Cd 25,Cd3 Count,Cd3 Count For Dli(Donor Lymphocyte Infusion),Cd3+Cd4+Cd8 Absolute Counts Profile,Cd34 Count,Cd4 Cd8 Count,Cd4 Count,Cd5 Count,Cdc73-Related Conditions Test - Cdc73,Cea,Cea Body Fluid,Cebpa,Cell Free Dna - Egfr (Del19+T790m+L858r) By Dd Pcr,Central Core Disease Test - Ryr1,Centromere Antibody,Centronuclear Myopathy Panel - Bin1, Ccdc78, Dnm2, Mtm1, R Yr1, Ttn, Myf6,Cerebral Cavernous Malformations Panel,Cerebral Creatine Deficiency Panel - Gamt, Gatm, Slc6a8,Cerebral Creatine Deficiency Syndrome 1(Ccds1),Ceruloplasmin,Cfu Level,Ch 50 (Total Hemolytic Complement),Charcot-Marie-Tooth Disease Autosomal Dominant Panel - 20 Genes,Charcot-Marie-Tooth Disease Autosomal Recessive Panel - 14 Genes,Charcot-Marie-Tooth Disease Comprehensive Panel - 32 Genes,Charcot-Marie-Tooth Disease X- Linked Panel- Aifm1, Gjb1, Pdk3, Prps1,Charcot-Marie-Tooth Disease Type 1A (Cmt1a ),Charge Syndrome,Chikungunia Igg,Chikungunia Igm (Rapid),Chikungunya Pcr,Chikungunya-Dengue Combo,Chlamydia Igg,Chlamydia Igg & Igm,Chlamydia Igm,Chloride,Chloride 24 Hour Urine,Cholesterol,Cholesterol Fluid,Cholinesterase Plasma/Serum,Cholinesterase Rbc,Chondrodysplasia Punctata 1, X- Linked Recessive (Cdpx1),Chondrodysplasia, Grebe Type,Choroideremia (Chm),Chromium,Chromogranin A,Chromosomal Deletion/Microdeletion Detection Panel,Chromosomal Microarray,Chromosome 17P Deletion,Chronic Granulomatous Disease, X-Linked (Cgd),Chronic Pancreatitis Panel - Casr, Cftr, Ctrc, Prss1, Spink 1,Chylomicrons,Ciliopathies Sensory Panel-39 Genes,Cladosporium Herbarum - Specific Igg,Cleft Palate, Isolated (Cpi),Cleidocranial Dysplasia (Ccd),Clinical Exome Sequencing Test,Clinical Exome Sequencing (8400 Genes),Cll Fish And Karyotyping Panel,Cll Fish Panel,Cll Panel,Clopidogrel Drug Sensitivity (Cyp2c19 Mutations),Clostridium Difficile Antigen (Gdh),Clostridium Difficile Toxin,Clostridium Difficile Toxin & Antigen,Clostridium Difficile Toxin Detection By Pcr-Genexpert,Clot Retraction,Clozapine Level,Cmpd Reflex Panel,Cmv Igg,Cmv Igm,Cmv-Qualitative Pcr,Cmv-Quantitation,Co2,Cobalt Blood,Coenzyme Q10-Coq10 Serum,Coffin-Lowry Syndrome (Cls),Cold Agglutinin Titre,Colorectal Cancer Panel - 23 Genes,Combined Hereditary Dementia And Amyotrophic Lateral Sclerosis Panel (Upto 27 Genes),Common Hereditary Cancers Panel (Breast, Gyn, Gi) - 42 Genes,Complement 3 (C3) Level,Complement 4 (C4) Level,Complement, Total (Ch50),Comprehensive Autosomal Dominant Cerebellar Ataxia Panel,Comprehensive Hereditary Cancer Panel - 34 Genes,Comprehensive Lung Cancer Panel (171 Genes),Comprehensive Muscular Dystrophy Panel - 49 Genes,Comprehensive Myopathy Panel-40 Genes,Comprehensive Neuromuscular Disorders Panel + Sod1,Comprehensive Neuromuscular Disorders Panel (Upto 121 Genes),Comprehensive Neuropathies Panel (Upto 83 Genes),Congenital Adrenal Hypoplasia (Cah),Congenital Fiber-Type Disproportion Panel- Acta1, Lmna, Myh7, Ryr1, Sepn1, Tpm2, Tpm3,Congenital Heart Disease Including Laterality Defects Panel - 72 Genes,Congenital Muscular Dystrophy Panel - 26 Genes,Congenital Myasthenic Syndrome Panel - 17 Genes,Congenital Myopathy Panel - 24 Genes,Constitutional Mismatch Repair- Deficiency Panel - Epcam, Mlh1, Msh2, Msh6, Pms2,Copper Level - Serum,Cornelia De Lange Syndrome 1 (Cdls1),Cornelia De Lange Syndrome 2 (Cdls2),Cornelia De Lange Syndrome Panel - Hdac8, Nipbl, Rad21, Smc1a, Smc3,Coronary Heart Disease Risk Factor - 9P21,Cortical Dysplasia-Focal Epilepsy Syndrome,Cortisol (4 Pm),Cortisol (8 Am),Cortisol (Random),Cortisol Stimulation By Acth,Costello Syndrome - Hras,Covid-19 Igg Ab (Sars-Cov-2 Igg ),Covid-19 Ab Total (Sars-Cov-2 Total .,Cowden Syndrome 1 (Cws1),C-Peptide (Post Prandial),C-Peptide (Fasting),C-Peptide (Random),Cpk-Mb,Cpk-Mb By Clia/Cmia,Cpk-Mm,Cpk-Total,Craniofacial Dysostosis With Short Stature,Craniofrontonasal Syndrome (Cfns),Craniosynostosis Panel-11 Genes,Craniosynostosis, Type 2 (Crs2),Crc (Colorectal) Targated Gene Panel,Creatinine,Creatinine Fluid,Creatinine With Egfr,Cri-Du-Chat Syndrome,Crp (C - Reactive Protein),Crp-Hs,Cryoglobulin,Cryptococcal Antigen- Csf,Cryptococcal Antigen-Serum,Culture And Sensitivity S Anaerobic,Culture And Sensitivity Ascitic Fluid,Culture And Sensitivity Bal Fluid,Culture And Sensitivity Blood Aerobic And Anaerobic By Bactalert/Bactec,Culture And Sensitivity Blood Aerobic By Bactalert/Bactec,Culture And Sensitivity Blood Anaerobic By Bactalert/Bactec,Culture And Sensitivity Blood By Conventional Method,Culture And Sensitivity Blood Fungal By Bactalert/Bactec,Culture And Sensitivity Body Fluid,Culture And Sensitivity Body Fluid Anaerobic By Bactalert/Bactec,Culture And Sensitivity Body Fluid By Bactalert/Bactec,Culture And Sensitivity Bone,Culture And Sensitivity Bone Marrow By Bactalert/Bactec,Culture And Sensitivity Bone Marrow Fungal By Bactalert/Bactec,Culture And Sensitivity By Bactalert/Bactec,Culture And Sensitivity Catheter Tip,Culture And Sensitivity Csf,Culture And Sensitivity Csf By Bactalert/Bactec,Culture And Sensitivity Cvp Tip,Culture And Sensitivity Ear Swab,Culture And Sensitivity Et,Culture And Sensitivity Eye Swab,Culture And Sensitivity Gonorrhea,Culture And Sensitivity Intralipid,Culture And Sensitivity Mott,Culture And Sensitivity Oral Secretion,Culture And Sensitivity Pancreatic Fluid,Culture And Sensitivity Pericardial Fluid,Culture And Sensitivity Pericardial Fluid Automated System With Mic Sensitivity,Culture And Sensitivity Pericardial Fluid Bactalert/Bactec,Culture And Sensitivity Peritoneal (Ascitic) Fluid,Culture And Sensitivity Peritoneal Fluid By Bactalert/Bactec,Culture And Sensitivity Pleural Fluid,Culture And Sensitivity Pleural Fluid By Bactalert/Bactec,Culture And Sensitivity Pus,Culture And Sensitivity Pus Anaerobic,Culture And Sensitivity -Rt Secretion,Culture And Sensitivity Semen,Culture And Sensitivity Sputum,Culture And Sensitivity Stool,Culture And Sensitivity Swab,Culture And Sensitivity Synovial Fluid,Culture And Sensitivity Synovial Fluid By Bactalert/Bactec,Culture And Sensitivity Throat Swab,Culture And Sensitivity Tissue,Culture And Sensitivity Tissue Anaerobic,Culture And Sensitivity Urine,Culture And Sensitivity Vaginal Swab,Culture And Sensitivity Wound,Csf - Cerebro Spinal Fluid Analysis,Csf - Glucose,Csf Protein,Csf Chikungunya Pcr,Csf Cytospin,Csf For Cytology,Csf For Measles Igg,Csf For Measles Igm,Csf Igg,Csf Igg Index,Csf Oligoclonal Band,Csf Protein,Csf Tpha,Csf Varicella Igg,Currarino Syndrome,Cyclosporine,Cyfra 21.1,Cystatin C,Cystic Fibrosis - Cftr (32 Mutations),Cystic Fibrosis - Cftr (Delta508 Mutation); With Maternal Cell Contamination Analysis,Cystic Fibrosis - Cftr (Delta508 Mutation),Cystic Fibrosis Test (Exonic Regions),Cystic Fibrosis-Cftr(32 Mutations) With Maternal Cell Contamination Analysis,Cysticercosis (Taenia Solium) Antibody Igg,Cysticercus(Taenia Solium) Igg,Cystinosis, Nephropathic (Ctns),Cystinosis, Nephropathic (Ctns) By Ngs,Cytomegalovirus Avidity Igg,D3-Hydroxybutyrate( Acetone) Serum,Dandy-Walker Syndrome (Dws),Danon Disease,Dct- Gel System,D-Dimer,Deafness, Autosomal Dominant 10 (Dfna10),Dengue Antigen And Antibody (Rapid),Dengue Igg (Elisa),Dengue Igm (Elisa),Dengue Ns1 Antigen (Elisa),Dengue Pcr,Dengue Profile (Elisa),Desmoglein (Dsg) 1 And 3Antibody,Desmoglein I & Iii Antibody,Detection Of Paraquat Urine,Dgp Iga (Deamidated Gliadin Peptide (Dgp) Antibodies (Anti-Dgp),Dgp Igg (Deamidated Gliadin Peptide (Dgp) Antibodies (Anti-Dgp),Dhea,Dhea-S,Dhr (Dihydrorhodamine) Assay,Diabetes Mellitus Autoantibody Panel Type -1,Diamond-Blackfan Anemia Panel-10 Genes,Dicer1 Syndrome Test,Digeorge Syndrome (Dgs),Digeorge Syndrome/Velocardiofacial Syndrome Complex-2,Digoxin,Dihydropyrimidine Dehydrogenase Deficiency,Dihydrotestosterone (Dht),Dilated Cardiomyopathy Panel,Diphtheria-Pertussis-Tetanus Antibody Panel Igg,Disorders Of Male Sex Development Panel - Nr0b1, Nr5a1, Sry, Ar, Srd5a2,Distal Myopathy Panel - 17 Genes,Dmd (26 Exons),Dmd (79 Exons),Dna Fragmentation Index/Ncd,Dna Isolation,Dna Profiling,Donor Of Lymphocyte Cross Match Report (Cdc),Donor Of T & B Cell Flow Cross Match (Fcxm) Report,Donor Specific Antibody (Dsa),Donor Specific Antibody (Dsa) By Luminex,Double Marker,Down Syndrome,Drug Susceptibility By Disk Diffusion,Duane-Radial Ray Syndrome (Drrs),Duane-Radial Ray Syndrome Test - Sall4,Dyggve-Melchior-Clausen Disease (Dmc),Dyskeratosis Congenita Panel- Ctc1, Dkc1, Nhp2, Nop10, Ter C, Tert, Tinf2,Dystonia Comprehensive Panel -18 Genes,Dystroglycanopathy Panel -17 Genes,Dystrophinopathies Test - Dmd,E2a,Early Infantile Epileptic Encephalopathy Panel - 43 Genes,Ebv Ea Igg,Ebv Ea Igm,Ebv Ebna Igg,Ebv Panel,Ebv Qualitative Pcr,Ebv Quantitative Pcr,Ebv Vca Igg,Ebv Vca Igm,Echinococcus (Hydatid Cyst) Igg,Ectodermal Dysplasia Panel- Eda, Edar, Edaradd, Wnt10a,Edwards Syndrome,Egfr,Egfr (Lung Cancer Nsclc),Egfr Mutation Analysis,Ehlers-Danlos Syndrome (Vascular) - Col3a1 (Targeted),Elane-Related Neutropenia Test,Electrolyte 24 Hour Urine,Electrolytes,Electrolytes Extended With Anion Gap,Electrolytes Urine,Electron Microscopy,Elt(Euglobulin Lysis Time),Ema Binding Test For Hereditary Spherocytosis,Emery-Dreifuss Muscular Dystrophy Panel- Emd, Fhl1, Lmna, Syne1, Tmem43,Ena Profile Qualitative Elisa (Extractable Nuclear Antigens (Ena),Ena Profile Quantitative By Elisa,Endomycial Antibody Iga,Endomycial Antibody Igg,Endomysial Antibody,Endotoxin Water,Eosinophilic Leukemia Panel(Pdgfra,Pdgfrb,Fgfr1 And Cbfb),Epilepsy Panel - 103 Genes,Epo (Erythyropoetion),Esr 1 Hour,Esr 2 Hour,Estradiol (E2),Estriol (E3 Level),Estriol Uncongugated (E3 Level),Everolimus Level,Examination For Pneumocystis Carinii,Exfoliative Cytology,Exosap-06 (Enzymatic Purification),Fabry Disease,Fabry Disease Test By Ngs,Factor Ii Assay,Factor Ii Mutation By Pcr,Factor Ii Mutation By Sanger,Factor Ix Assay,Factor V Assay,Factor V Leiden Mutation By Pcr,Factor V Leiden Mutation By Sanger,Factor Vii Assay,Factor Viii Assay,Factor X Assay,Factor Xi Assay,Factor Xii Assay,Familial Acute Myeloid Leukemia With Mutated Cebpa Test - Cebpa,Familial Adenomatous Polyposis 1 (Fap1),Familial Adenomatous Polyposis - Apc,Familial Cutaneous Melanoma - Cdk4, Cdkn2a,Familial Dysautonomia Test,Familial Dysautonomia Test - Ikbkap,Familial Gastrointestinal Stromal Tumor Syndrome Panel- Kit, Nf1, Pdgfra, Sdha, Sdhb, Sdhc, Sdhd,Familial Hypercholesterolemia - Apob, Ldlr, Ldlrap1, Pcsk9,Familial Neuroblastoma Panel- Alk, Phox2b, Kif1b,Familial Thrombocytopenia With Propensity To Acute Myelogenous Leukemia- Runx1,Fanconi Anemia Panel - 17 Genes,Fasting Blood Sugar (Fbs),Fasting Urine Sugar,Fatty Acid Oxidation Defects Panel-17 Genes,Fbg/F Insulin Ratio,Fdp,Fecal Elastase,Feingold Syndrome 1 (Fglds1),Ferritin,Fgfr3-Related Disorders Test,Fibrinogen,Fibrinogen Degradation Product (Fdp),Fibroblast Growth Factor 23,Filaria Antigen,Fip1l1-Pdgfra Gene Rearrangement,Fish - Cdkn2a/Cep 9,Fish - Cep 8 ( Trisomy 8),Fish - Del 17P On Cd 138 Enriched Plasma Cells,Fish - Igh Gene Rearrangement,Fish Panel For Ph Like All,Fish 1P/19Q,Fish Abl1 Gene Rearrangement,Fish Abl2 Gene Rearrangement,Fish Abortus Material (13 18 21 X & Y),Fish Alk Gene Rearragngement,Fish Aml/Eto T(8;21),Fish Bcl1 /Igh T(11;14) (Mantle Cell Lymphoma) - Paraffin Block,Fish Bcl1/Igh T(11;14) (Mantle Cell Lymphoma) Bone Marrow,Fish Bcl2 Gene Rearrangement Bone Marrow,Fish Bcl2 Gene Rearrangement Paraffin Block,Fish Bcl6 Gene Rearrangement Bone Marrow,Fish Bcl6 Gene Rearrangement Paraffin Block,Fish Bcr/Abl T(9;22),Fish C Myc Gene Rearrangement Paraffin Block,Fish C Myc Gene Rearrangement Bone Marrow,Fish Cep Xy (Chimerism),Fish Crlf2 Gene Rearrangement,Fish Del 13Q,Fish Del 15Q11/15Q24 (Prader Willi Syndrome),Fish Del 17P / Del 11Q,Fish Del 1P32.2(Cdkn2c)/ Amp 1Q21.3-Q22(Cks1b),Fish Del 20Q,Fish Del 22Q11/22Q13 (Digeorge Syndrome),Fish Del 5Q,Fish Del 7Q,Fish Fgfr1 Gene Rearrangement,Fish Fgfr3/Igh T(4;14),Fish For Bcl2::Igh Gene Rearrangement / T(14;18),Fish For Chromosome 21 (Trisomy 21),Fish For Chromosome 13 18 & 21,Fish For Chromosome 13 & 21,Fish For Chromosome 18 & 21,Fish For High Grade Lymphoma Panel( Bcl2/Bcl6/C Myc ) Paraffin Block,Fish For High Grade Lymphoma Panel( Bcl2/Bcl6/C Myc ) Bone Marrow,Fish For Myeloma [Del 13Q Del 11Q Del 17P T(11:14) T(4;14) T(14;16) Del 1P/Amp1q],Fish Foxo1 Gene Rearrangement,Fish Her2 Neu,Fish Inv(16),Fish Jak2 Gene Rearrangement,Fish Maf/Igh T(14;16),Fish Met Gene Amplification,Fish Mll Gene Rearrangement,Fish Mye0v/Igh T(11;14),Fish N Myc Gene Amplification,Fish On Cd 138 Enriched Plasma Cell For Multiple Myeloma,Fish Pdgfr Alpha,Fish Pdgfr Beta,Fish Pml/Rara T(15;17),Fish Ret Gene Rearrangement,Fish Ros1 Gene Rearrangement,Fish Semen (13 18 21 X & Y),Fish Synovial Sarcoma (Ss-18 Gene),Fish T(1;19) E2a/Pbx1,Fish Tel/Aml T(12;21),Fish Trisomy 12,Fish-Ewings Sarcoma (Ewsr1 Gene Rearrangement),Flt3 Mutation,Flu/H1n1 2009,Fluid Albumin,Fluid Amylase,Fluid Bile Salt And Bile Pigment,Fluid Cea,Fluid Cell Count,Fluid Chloride,Fluid Creatinine,Fluid For Afb,Fluid For Cytology,Fluid For Cytology With Cell Block,Fluid For Protein,Fluid Gram And Z N Stain,Fluid Ldh,Fluid Lipase,Fluid Routine Examination,Fluid- Sugar,Fnac - (Prepared 6 Slides),Fnac Slides For Review (13 - 18 Slides),Fnac Slides For Review (19 - 24 Slides),Fnac Slides For Review (25 - 30 Slides),Fnac Slides For Review (31 Slides),Fnac Slides For Review (6 - 12 Slides),Fnac Slides For Review (Up To 6 Slides),Focal Dermal Hypoplasia (Fdh),Folate (Folic Acid) Rbc,Folic Acid,Food Intolerance Profile,Forebrain Defects,Foundation One Cdx (F1cdx),Foundation One Heme,Foundation One Liquid Cdx (F1lcdx),Fractional Excretion Of Sodium (Fena),Fragile X - Female,Fragile X - Male,Fragile X (Repeat Expansion Analysis) - Fmr1,Fragile X Mental Retardation Syndrome,Free Androgen Index,Free Beta Hcg,Free Cortisol - 24 Hrs Urine,Free Hemoglobin (Plasma Hemoglobin),Free Kappa Light Chain,Free Lambda Light Chain,Free Light Chain Assay,Free Protein S,Free Psa,Free Testosterone,Friedreich Ataxia Mutation Analysis,Frontotemporal Dementia Panel (Upto 13 Genes),Frozen Section (Intra Operative),Fructosamine,Fsh,Ft3 (Free T3),Ft4 (Free T4),Fungal Culture,Fungal Mic By Broth Dilution,Fungus Identification,Fungus Identification And Sensitivity,Fungus Sensitivity,G6pd Qualitative,G6pd Quantitative,Gad 65 Antibody (For Paraneoplastic Syndrome),Galactosemia Quantitative,Galactosemia Panel- Gale, Galk1, Galt,Ganglioside Antibody Igg And Igm,Gastric Cancer Panel - 19 Genes,Gastric Juice For Hemosiderophage,Gastrin Level,Gata1-Related X-Linked Cytopenia Test,Gata2 Deficiency Test,Gelex-07 (Gel Extraction),Genesynthesis-1 (436 Base Pair-1 Kb),Genesynthesis-10 (6-10 Kb),Genesynthesis-2 (1-2 Kb),Genesynthesis-3 (2-3 Kb),Genesynthesis-4 (3-4 Kb),Genesynthesis-6 (4-6 Kb),Germline Cancer Panel,Ggt,Gh (Growth Hormone),Gh Stimulation Test,Giardia Ag Stool,Giemsa Stain,Gilbert Syndrome,Gli3-Related Disorders Test,Gliadin Iga,Gliadin Igg,Gliadin Igg & Iga Profile,Glioma Comprehensive Panel,Glioma Extended Diagnostic & Prognostic Panel,Glioma Molecular Panel,Glucose Fluid,Glucose Transporter Type 1 Deficiency Syndrome Test- Slc2a1,Glucose-6-Phosphate Dehydrogenase Deficiency Test- G6pd,Glutaric Acidemia Type I Test - Gcdh,Glycerol Kinase Deficiency,Gms Stain,Gonorrhoea - Microscopy,Gram Stain,Greig Cephalopolysyndactyly Syndrome (Gcps),H. Pylori Ag Stool,H. Pylori Iga,H. Pylori Igg,H.Pylori Igm,Ham Test,Hanging Drop Preparation,Hanta Virus Igm-Antibodies,Haptoglobin,Hav Antibody Igm (Rapid),Hav Igm,Hav-Igg,Hb Electrophoresis - Hplc,Hb Electrophoresis By Capillary,Hb H Preparation,Hba1c (Glycosylated Hemoglobin),Hba1c By Turbidimetry,Hba1c (Hplc),Hbeag,Hbsag By Elfa,Hbsag Cmia,Hbsag Elisa,Hbsag Rapid,Hbsag-Quantitative (End Point Titre),Hbv By Taqman,Hbv Drug Resistance (Hbv Quantitative Values Mandatory),Hbv Genotyping (Hbv Quantitative Values Mandatory),Hbv Genotyping And Drug Resistance Mutations (Hbv Quantitative Values Mandatory),Hbv-Qualitative Pcr,Hbv-Quantitation,Hco3 (Bicarbonate),Hcv Genotyping (Hcv Quantitative Values Mandatory),Hcv Igm,Hcv Quantitative And Genotyping,Hcv Rna-Quantitation,Hcv-Qualitative Pcr,Hdl Cholesterol,Hdv (Hepatitis Delta Virus) Qualitative,Hdv Igm,He4 Roma Index,He4 -Roma Index Human Epididymis Protein-4 Serum,He4 With Roma Index,Heavy Metals (Nine Panel),Heinz Bodies,Hematocrit-Fluid,Hemochromatosis (Targeted) - Hfe,Hemophilia (A&B) And Von Will Brad Disease Workup,Hemophilia A (Hema),Hemophilia B (Hemb),Hemophilia Complete Workup (F8 & F9 Gene Sequencing + F8 Intron 22 & 1 Inversion),Heparin Induced Thrombocytopenia (Hit Testing),Hepatitic C Virus (Hcv) - Rapid,Hepatitis B Virus (Hbv) Genotypes & Drug Resistance,Hepatitis D Virus ( Hdv) Antibody- Total,Hepcidin Level,Her2 (Erbb2) (Equivocal) By Fish,Her-2 Neu (H2n),Hereditary Alzheimers Disease Panel (3 Genes),Hereditary Breast Cancer (High Risk Panel) - Brca1, Brca2, Cdh1, Palb2, Pten, Stk11, Tp53,Hereditary Breast Cancer (Extended Panel)- 17 Genes,Hereditary Breast Cancer (Moderate Risk Panel) - 10 Genes,Hereditary Cancer Risk Assessment - 30 Genes,Hereditary Colon Cancer - 14 Genes,Hereditary Diffuse Gastric Cancer Syndrome- Cdh1,Hereditary Fructose Intolerance- Aldb,Hereditary Gynecologic Cancers (High Risk Panel)- Brca1, Brca2, Epcam, Mlh1, Msh2, Msh6, Pms2, Pten, Tp53,Hereditary Hemochromatosis Panel - Hamp, Hfe, Hfe2, Slc40a1, Tfr2,Hereditary Hemorrhagic Telangiectasia Panel - Acvrl1, Eng, Rasa1, Smad4, Gdf2,Hereditary Hyperparathyroidism Panel- Casr, Cdc73, Cdkn1b, Men1, Ret,Hereditary Leiomyomatosis And Renal Cell Cancer Test - Fh,Hereditary Motor Neuropathy Panel,Hereditary Papillary Renal Cell Cancer - Met,Hereditary Paraganglioma- Pheochromocytoma Panel - 14 Genes,Hereditary Parkinsons Disease And Parkinsonism Panel (Upto 17 Genes),Hereditary Prion Disease Test,Hereditary Sensory And Autonomic Neuropathy Panel (Upto 17 Genes),Hereditary Spastic Paraplegia Autosomal Dominant Panel - 12 Genes,Hereditary Spastic Paraplegia Autosomal Recessive Panel - 27 Genes,Hereditary Spastic Paraplegia X- Linked Panel- Kdm5c, L1cam, Plp1, Slc16a2,Hereditary Spastic Paraplegia Comprehensive Panel - 43 Genes,Hereditary Thrombophilia Panel- F2, F5, Proc, Pros1, Serpinc1, F9, Mpl,Herpes Zoster - Igg,Herpes Zoster - Igg & Igm,Herpes Zoster - Igm,Heterotaxy - Ccdc39, Ccdc40, Foxh1, Gdf1, Nodal, Zic3,Heterotaxy, Visceral, 1, X-Linked (Htx1),Hev Antibody Igm (Rapid),Hev- Igg,Hev-Igm,Hexosaminidase 1 Level,Hirschsprung Disease, Susceptibility To, 1 (Hscr1),Hirschsprung Disease, Susceptibility To, 2 (Hscr2),Histo Pathological Examination Of Renal Biopsy Allograft + C4d (Without If),Histo Stain - Any Special Stain,Histo Stain - Congo - Thio T,Histo Stain - Thio-T,Histopathological Examination Of Kidney Biopsy With Special Stains & Immunofluorescence,Histopathological Examination Of Nerve With Special Stains,Histopathological Examination Of Skin With Immunofluroscence,Histopathology Slide-1,Histopathology Slide-10,Histopathology Slide-11,Histopathology Slide-2,Histopathology Slide-3,Histopathology Slide-4,Histopathology Slide-5,Histopathology Slide-6,Histopathology Slide-7,Histopathology Slide-8,Histopathology Slide-9,Hiv By Rapid,Hiv & Hbsag By Cmia,Hiv Duo (Elfa),Hiv Genotyping And Drug Resistance Mutations,Hiv I & Ii - Rapid,Hiv I & Ii By Cmia,Hiv I & Ii By Eclia,Hiv I & Ii Elisa,Hiv Proviral Dna Load Pcr,Hiv Western Blot,Hiv-1 Rna -Quantitation,Hiv-Qualitative Pcr,Hla B27,Hla B27 By Flowcytometry,Hla Typing + Cross Match,Holo Tc (Holo B12)- Holotranscobalamin,Holoprosencephaly (Hpe) Panel,Holoprosencephaly Panel - Gli2, Shh, Six3, Tgif1, Zic2,Holt-Oram Syndrome (Hos),Holt-Oram Syndrome Test - Tbx5,Homa Index Insulin Resistance Test,Homa Ir Insulin Resistance Index,Homocysteine Serum,Homocysteine Urine,Homocystinuria Panel - Cbs, Mmachc, Mmadhc, Mtrr,Hpv High Risk Typing,Hpv Qualitative 16/18 Typing,Hs -Crp,Hsv I & Ii Igg,Hsv I & Ii Igm,Hsv I Igg,Hsv I Igg & Igm,Hsv I Igm,Hsv Ii Igg,Hsv Ii Igg & Igm,Hsv Ii Igm,Hsv1 And Hsv2-Qualitative,Hsv1 And Hsv2-Quantitation,Htlv I & Ii Serum,Huntington Disease,Hyperkalemic Periodic Paralysis Panel,Hyperparathyroidism Panel- Casr, Cdc73, Cdkn1b, Men1, Ret,Hyperphenylalaninemia Panel - Gch1, Pah, Pcbd1, Pts, Qdpr,Hyperprolinemia Panel - Aldh4a1, Prodh,Hypersensitivity Pneumonitis Panel Serum,Hypertrophic Cardiomyopathy Panel,Hypoparathyroidism, Sensorineural Deafness And Renal Disease,Hypophosphatemic Rickets, X-Linked Dominant (Xlhr),Hypotonia-Cystinuria Syndrome,Ia2 Insulin Autoantibodies Clia,Ichthyosis, X-Linked (Xli),Ict (Indirect Coombs Test) - Gel System,Ict (Indirect Coombs Test)- Tube Agglutination,Idh Mutations,Iga,Igd Heavy Chain (Surface),Ige,Igf Bp-3,Igf Bp3,Igf-1,Igg,Igg Subclasses 1-4,Igg1,Igg2,Igg3,Igg4,Igh Rearrangement,Igh Rearrangement T(11;14), T(4;14), T(14;16),Igm,Igm Rheumatoid Factor,Igvh Gene Mutation,Ihc Any Single Marker,Ihc Any Single Marker With Reporting,Ihc Any Three Markers,Ihc Any Two Markers,Ihc C4d (Ihc/If),Ihc Er Pr,Ihc Er Pr Her2 Neu Ki67+Reflex Fish Her2neu,Ihc Er Pr Her2 Neu+Reflex Fish Her2neu,Ihc Er Pr Her2-Neu,Ihc Er Pr Her2-Neu Ki67,Ihc Extended Panel,Ihc Her-2 Neu,Ihc In Situ Hybridization (E-Ber),Ihc Msi,Ihc Msi (Ho),Ihc Panel,Ihc Panels With Reporting Er Pr C-Erb-B2(Her2 Neu) - 720,Ihc Pdl1 By Dako (22C3),Ihc Ros1(Lung Marker),Ihc Staining,Ihc Up To 5 Markers,Imatinib Resistance Mutation Analysis (Irma),Immature Platelet Fraction (Ipf),Immunofixation Electrophoresis 24 Hours Urine,Immunofixation Electrophoresis Complete Panel With B-2 Micr,Immunofixation Electrophoresis Qulalitative,Immunofixation With Protein Electrophoresis,Immunoglobulin Profile,Immunophenotyping - Leukemia Panel,Immunophenotyping - Lymphoma Panel,Immunophenotyping Ema Dya Binding Test,Immunophenotyping For Alps,Immunophenotyping For Leukocyte Adhesion Defect -I,Immunophenotyping For Mrd,Immunophenotyping For T Cell Subset,Immunophenotyping For Myeloma,Immunophenotyping For Platelet Function Test,Immunophenotyping Leukemia Panel In Body Fluid,Immunophenotyping Leukemia Panel,Immunophenotyping Leukemia/Lymphoma(Clpd),Inclusion Body Myopathy Panel (Upto 5 Genes),Incontinentia Pigmenti (Ip),Indian Ink Examination For Cryptococcus Neoformans,Infectious Mononucleosis,Inflammatory Bowel Disease (Ibd) Differentiation Panel,Influenza A Igg,Influenza A Igg Antibody,Influenza A Igm,Influenza B Igg Antibody,Inhibin A,Inhibin B,Inhibitor Assay Study,Inhibitors Screen,Insulin (Fasting),Insulin (Pp),Insulin (Random),Insulin 1 Hour After Glucose,Insulin 2 Hour After Glucose,Insulin Antibody,Interleukin 6,Intrinsic Factor Antibody,Inv (16),Iodine Serum,Ionized Calcium,Ipt - Aml Mrd(Mrd- Measurable Residual Disease),Ipt - B All Mrd,Ipt - Clpd Mrd( Clpd-Chronic Lymphoproliferative Disorders,Ipt - Leukemia Panel / Lymphoma Panel,Ipt - Multiple Myeloma Mrd,Ipt - Myloma Panel,Ipt - T All Mrd,Ipt- Alps Panel,Iridogoniodysgenesis, Type 1 (Irid1),Irma By Ngs,Iron,Iron Profile,Iron Stain,Islet Cell Antibodies By Clia,Islet Cell Antibodies By Ifa,Isolated & Syndromic Congenital Heart Disease Panel -55 Genes,Isolated Gonadotropin- Releasing Hormone Deficiency Panel - Anos1, Chd7, Fgfr1,Isoniazid By Hplc
