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Detection of genetic polymorphisms associated with impaired folate cycle

on request
Detection of genetic polymorphisms associated with thrombophilia risk

on request
Genetics of hereditary diseases. Deletions of AZF-locus

on request
Genetics of hereditary diseases. Musoviscidosis screening

on request
Karyotyping

on request
DNA diagnosis of the syndrome Martin-Bell or Fragile-X

on request
DNA diagnosis spinal muscular atrophy

on request
HLA-typing (2 people)

on request
DNA diagnosis of phenylketonuria

on request
Determination of the karyotype in chorionic villi abortive material

on request
Semen analysis, FISH-method

on request