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Our Molecular Genetics Laboratory offers DNA analysis for diagnosis and carrier testing for metabolic and other genetic disorders. The results are reviewed and interpreted by board certified cytogeneticists. Molecular cytogenetic analyses are offered using fluorescence in situhybridization (FISH) and chromosomal SNP (single nucleotide polymorphism) array.
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Our Cytogenetics Laboratory offers comprehensive chromosomal analysis on peripheral blood, skin biopsies, products of conception, bone marrow and malignant tissues. Our biochemical genetic specialists provide comprehensive interpretation of test results and recommendations about medical follow-up and/or further testing. Our Biochemical Genetics Laboratory performs a variety of analyses using gas chromatography/mass spectroscopy (GC/MS), high performance liquid chromatography (HPLC), tandem mass spectrometry (MS/MS) and enzyme analyses in various tissues for the diagnosis and monitoring of patients with inborn errors of metabolism. Genetics Test Lookup Biochemical Genetics Laboratory