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Molecular Cytogenetics

 
Fluorescent In Situ Hybridization (FISH) technique is used to detect numerical as well as minor structural rearrangements on all the above tissues to confirm or identify a known genetic problem prior discussion with the lab is essential.
Currently it is available for fetal aneuploidy, micro-deletion syndromes and oncology mainly haematological malignancies.
 
 
ANEUPLOIDY SCREEN
13,18,21 and sex
chromosomes
Prenatal and postnatal, sperm, oocytes
and blastomere
   
ONCOLOGY
BCR / ABL In CML
PML / RARA In APML
13q 14 region Retinoblastoma
   
MICRODELETIONS
SRY PROBE Ambiguous genitalia & Sex Chromosomal abnormalities
Di George probe and other micro deletions CHD
Chromosome breakage syndrome Faaconi's Anemia, Bloom's Syndrome, Ataxia Talengectasia, Xeroderma Pigmentosa
 
Our Services
Genetic Screening
Genetic Counseling
Genetic Screening
Cytogenetic Testing
Molecular Cytogenetics

Stem Cell Cytogenetics

Prenatal Diagnostic Services
Paediatric Cytogenetics
Metabolic Studies
Adult Genetic Disorders
Cancer Cytogenetics
Genotoxicity Studies
Organ System Diseases
DNA Diagnostic Services
Training and Career Guidance
 
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