At LIFE CODE, we employ the most advanced methodologies for highly specialized analysis of collected specimens, encompassing both hereditary and non-hereditary disorders. Please refer to our detailed catalog for a complete overview.
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Molecular Diagnosis of Cystic Fibrosis
Cystic fibrosis (CF), also known as mucoviscidosis, is the most
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Molecular Testing for α-Thalassemia
Thalassemia is a monogenic disorder inherited in an autosomal recessive
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Molecular Testing for β-Thalassemia and Sickle Cell Anemia
Thalassemia is a monogenic disorder inherited in an autosomal recessive
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Molecular Testing for Hemophilia
Hemophilia is an X-linked recessive genetic disorder affecting coagulation factor
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Molecular Testing for Fragile X Syndrome (FRAXA/FRAXE)
Fragile X syndrome is the most common genetic disorder associated
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Molecular Diagnosis of Rare Inherited Disorders
The analysis of rare inherited disorders is performed using Whole
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Molecular Testing for Non-Syndromic Hearing Loss
Non-syndromic hearing loss occurs in approximately 1 in 1,000 newborns.
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Molecular Karyotyping (Array CGH)
Molecular karyotyping is a valuable tool for detecting and mapping
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Sperm Apoptosis / DNA Fragmentation Analysis
Sperm DNA can be damaged due to oxidative stress caused