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Services : Diagnostic Services : Cytogenetic Services

[In collaboration with ‘Foundation for Research in Genetics & Endocrinology’ (FRIGE)]
  • Abortus material (long term culture)
  • Amniotic fluid cell culture
  • Ataxia- Talengiactasia Mytocin assay
  • Blood chromosomes
  • Bone marrow chromosomes
  • Chord- blood prenatal chromosomes
  • Fanconi’s anaemia- mitomycin assay
  • Fibroblast culture for other tests
  • Fragile X syndrome- Thymidine block
  • Prader Willi syndrome- microdeletion (Chm 15)
 
  • Recurrent abortions
  • CF25 muttationDeletion-22q deletion
  • DMD carrier test carrier test linkage studies
  • DMD deletion testing
  • DMD prenatal diagnosis
  • Fragile X methylation
  • Hemophilia
  • Rett syndrome MECP2 sequencing
  • Spinal muscular atrophy
  • Y- chromosome deletion
  • Chromosome Linkage Study
    Molecular cytogenetics
  • ABL/BCR
  • XX/XY: Sex matched BM transplantation
  • Digeorge syndrome
  • WCP- 21q: for trisomy 21

    Biochemical genetics
  • Galactosemia
  • Lactate/ pyruvate/ ammonia
  • Phenyl alanine ketonurea
  • Urine porphyrine

Enzyme

alpha glucosidase, arylsulphatase A-MLD, arylsulphatase B (MPS typeVI), Beta glucoronidase (MPS VII), Beta Hexosaminidase, Fucosidase, beta glucosidase- gaucher disease, beta galactosidase, iduronidase- Hurler syndrom, Mannosidase A & B, MPS II- Hunter syndrome, MPS IVA – Morquio desease,Sphingomyelinase- Niemann – Pick’s desease, N- Acetyl- alpha- glucoseaminidase- MPS III.
  • Prenatal diagnosis of biochemical disorders.

With the advent of molecular biology and dramatic improvement in clinical biochemistry, microbiology and allied sciences, the horizons for helping mankind for better health and prosperity have broadened like never before. We, at geneOmbio Technologies look this as an opportunity to embark into the world of Biotechnology with a vision of providing the most recent tools of biology for the well-being and prosperity of our society.

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