U N Mehta Institute Of Cardiology & Research Center - Gujarat
41256571 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...