| GENETIC LAB | Private ward - Rs | OPD & General Ward charges - Rs |
| 4 CONNEXIN 26 MUTATIONS | 1000 | 1000 |
| ACHONDROPLASIA | 1000 | 1000 |
| AMNINOTIC | ||
| AMNIOTIC FLUID AFP ASSAY | 300 | 300 |
| AMNIOTIC FLUID OR URINE 2 D | 750 | 750 |
| ANGELMAN SYNDROME | 1500 | 1500 |
| BLOOD/BONE MARROW FOR CHROMOSOMES | 750 | 750 |
| BUCCAL SMEAR FOR SEX CHROMATIN | 30 | 30 |
| CARIER SCREENING BY LINKAGE STUDIES IN DMD | 2000 | 2000 |
| CARRIER DETECTION OF DMD/HEMOPHILLIA/DNA DIAGNOSIS | 2000 | 2000 |
| CARRIER SCREENING FOR THALASSEMIA NESTROFF AND HB A2 | 300 | 300 |
| CHEMICAL TEST IN URINE | 80 | 80 |
| CHROMOSOMAL STUDY OF BLOOD/BONE MARROWKARYOTYPING | 500 | 500 |
| CHROMOSOMES FROM ABORTUS TISSUE | 2500 | 2500 |
| CHROMOSOMES FROM CVS BY CULTURE, OR BY CULTURE FOR | 2500 | 2500 |
| CORD BLOOD SAMPLING (KARYO TYPING + KLEHURS TEST) | 750 | 750 |
| CROMOSOMAL BREAKAGE STUDY OF BLOOD | 750 | 750 |
| CVS FOR SEXING FOR X-LINKED DISEASE | 1500 | 1500 |
| DELETION STUDIES IN DMD | 2000 | 2000 |
| DMD HEMOPHILIA, OR ENZYME | ||
| DNA BASED MUTATION DETECTION IN THALASSEMIA | 2000 | 2000 |
| DNA BASED MUTATION DETECTION ON DMD OR OTHER DISEASES | 3500 | 3500 |
| DNA STUDIES IN SMA | 1500 | 1500 |
| DNA STUDY IN CF (DELTA 508 AND INTRON 19 MUTATION) | 1000 | 1000 |
| DNA STUDY IN CF (FURTHER STUDY) MULTIPLEX TEST | 2000 | 2000 |
| Private ward - Rs | OPD & General Ward charges - Rs | |
| ELECTRONIC CELL COUNT | 150 | 150 |
| ELECTROPHORESIS FOR MPS AMNIOTIC FLUID ACETYLE | 750 | 750 |
| ESTRIOL | 200 | 200 |
| FOR ALL | 1000 | 1000 |
| FOR HURLUR | 2000 | 2000 |
| GALACTOSEMIA QUANTITATIVE ENZYME ASSAY | 750 | 750 |
| GALACTOSEMIA SCREENING [BEUTLER SPOTR FLORENSCENC TEST] | 500 | 500 |
| GENETIC KARYOTYPING | 500 | 500 |
| HYPO CHONDROPLASIA | 1500 | 1500 |
| LEUCOCYTE ENZYME ASSAY ARYLSULFATASE A, HEMOSAMINDASE | 750 | 750 |
| LEUCOCYTE ENZYME ASSAY FOR HURLUR (MPS) | 2000 | 2000 |
| LEYCOCYTE ENZYME ASSAY WITH CONTROL ENZYMES | 1000 | 1000 |
| MATERNAL SERUM AFP ASSAY | 150 | 150 |
| MATERNAL SERUM HCG ASSAY | 300 | 300 |
| MPS 24 HRS,ESTIMATION WITH CREATININE | 300 | 300 |
| MPS SPOT TEST ON URINE | 80 | 80 |
| PHYNOTYPIC CHERATERIZATION BY ISO ELECTRIC FOCUSING FOR ALFA 1 ANTITRIPSIN DEFICIENCY | 750 | 750 |
| PLASMA/URINE QUANTITATIVE AMINOSCIDS | 1500 | 1500 |
| PRADER WILLI | 1500 | 1500 |
| PRENATAL DIAGNOSIS BY ENZYME ASSAY | ||
| PRENATAL DIAGNOSIS OF ATAXIA | 6000 | 6000 |
| PRENATAL DIAGNOSIS OF HAEMOPHILLIA A and B | 2000 | 2000 |
| PRENATAL DIAGNOSIS OF SMA | 1500 | 1500 |
| PRENATAL DIAGNOSIS OF THALASSEMIA | 2000 | 2000 |
| PRENETAL DIAGNOSIS OF DMD BY DELETION STUDIES | 2000 | 2000 |
| RH GENOTYPING OF BLOOD/AF | 1000 | 1000 |
| SERUM AMMONIA | 125 | 125 |
| TELENGIECTASIA OR FRAGILE X PCR | 1000 | 1000 |
| THANATROPHIC DWARFISM | 1500 | 1500 |
| TRIPLE SCREENING TEST[MSAFP,BETA HCG, ESTRIOL] | 500 | 500 |
| URINARY SUCCINYL ACETONE ESTIMATION FOR TYROSENEMIA | 750 | 750 |
| URINE/PLASMA AMINOACID SCREENING /CHROMATOGRAPHY | 200 | 200 |
| XMM POLYMORPHISM STUDY | 1000 | 1000 |