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ADN Clinic ensure to patients life-long support for medical diagnosis in collaboration with leading providers of innovation technologies in genetic testing.
Providing to our patients life-long support for medical diagnosis in collaboration with leading providers of innovation technologies in genetic testing. We aim to set the basis for early diagnosis, inherited diseases predisposition and prevention therapies.
NIPT is a non-invasive test that detects genetic conditions such as Down, Edwards, and Patau syndrome, from as early as week 10 of pregnancy.
Detection of cancer-related biomarkers has become a fundamental step for a personalized treatment approach in cancer patients.
Cytogenetics is essentially a branch of genetics but is also a part of cell biology/cytology (a subdivision of human anatomy)
Molecular cytogenetics combines two disciplines, molecular biology and cytogenetics, and involves the analyzation of chromosome structure to help distinguish normal and cancer-causing cells.
Test for 24 types of hereditary cancers The most comprehensive cancer risk test lets you look into up to 79 genes and learn your genetic risk of developing breast, ovarian, prostate, colorectal, and other types of cancers with a simple and safe saliva-based test.
Paternity testing provides scientific evidence of whether a man can be a child's biological father. Paternity is determined by comparing the child's DNA with the DNA profile of the alleged father.
Genetic structures which are necessary for a healthy and functional body, are present in the nucleus of the cells making up the whole body.
Whole Exome Sequencing (WES) is a comprehensive genetic test that identifies changes in a patient's DNA that are causative or related to their medical concerns.
Whole genome sequencing (WGS) identifies almost all changes in a patient's DNA by sequencing both the entire protein coding and the non-coding regions of the genome.
Male and female infertility testing Knowing the exact cause of infertility allows for better diagnostic decisions, and enables enhanced counseling for parents with regard to risks for their children.
Newborns and children under 24 months presenting with life-threatening conditions need a fast and precise diagnosis to ensure rapid and efficient further diagnostic and therapeutic initiation.
Current developments in genetics enable geneticists to perform genetic tests on the embryo by means of in vitro fertilization (IVF) technique.
