GENETIC DIAGNOSIS SERVICE
The use of Array-CGHs allows the obtaining of a Molecular Karyotype with a resolution at least 10 times higher than the conventional karyotype. Obtaining the molecular karyotype is indicated in patients with idiopathic mental retardation, autism, and/or congenital malformations, to detect or rule out the presence of genomic material that defines the observed phenotype.

Choosing the most appropriate Array-CGH must be done individually, based on the objective of the study indicated for each patient. All the Array-CGHs used in the Genetic Diagnosis service allow the complete scanning of the genome, but with different degrees of resolution depending on the number of probes included in the platform and, in specifically designed arrays, also depending on the disease under study. Our team of professionals offers personalized customer service, proposing the most appropriate platform for each study.

Our Genetic Diagnosis service is adapted to the needs of specialist doctor and/ or professionals within the field of medical genetics.

NIMGenetics offers two types of services, depending on the professional’s needs: