Catalog

The LCG has different array resolutions in order to identify Copy number variations (CNV) and detection of loss of heterozygosity. This diagnosis can be done on pre-natal and post-natal samples.

LCG provides solutions in Genomics, Conventional and/or Molecular Cytogenetics and Molecular Biology for genetic studies of Developmental Disorders.

These studies are carried out taking into account the alterations present in the index case, using the most appropriate techniques in the set of existing LCG techniques to characterize the alterations.

Array-CHG

The LCG performs a wide variety of exams in Prenatal. The fetal genome can be analyzed more widely, by molecular karyotype (aCGH) and constitutional karyotyope, More specific techniques like FISH, MLPA and MS-MLPA can also be performed whenever necessary.

Annual 5-day course divided into theoretical, theoretical-practical sessions and 6 practical workshops, with the aim of addressing the evolution from cytogenetics to genomics, both in pre- and postnatal diagnosis and in research and forensic medicine