Genomic Disorders and Chromosome Rearrangements research program is focused on the study of chromosomal anomalies, more specifically on structural alterations and associated diseases.

​

Through the analysis and characterization of these anomalies, we aim to contribute to a greater knowledge of the Human Genome and to improve the prediction and prevention of the phenotypical consequences of anomalies such as translocations and inversions, detected through pre- and post-natal diagnosis.

​

​

Currently we have an ongoing project in cooperation with the Harvard Medical School called

 

"Next-Gen Cytogenetics Enters Clinical Care and Annotates the Human Genome"

​