O. Moreno-Niño

CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease

I. Zarante, Tatiana Pineda, A. Paredes, 2021, Clinical Medicine Insights. Cardiology.

Disorders of sex development: Genetic characterization of a patient cohort

F. Suárez-Obando, N. Fernández, J. Prieto, 2019, Molecular medicine reports.

Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX Caracterización citogenética y molecular en tejido gonadal de pacientes con síndrome ovotesticular y disgenesia gonadal 46,XY y 46,XX

F. Suárez, Camila Céspedes, Catalina Forero, 2021 .

22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate

Gloria L. Porras-Hurtado, Jorge Rojas, I. Zarante, 2019, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

22 q 11 . 2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and / or Palate

Gloria L. Porras-Hurtado, Jorge Rojas, I. Zarante, 2018 .

Chromosomal and SRY gene findings by FISH in patients with disorders of sexual development

N. Fernández, I. Zarante, Ana Clavijo, 2021, Revista Mexicana de Urología.

Cytogenetic and molecular characterization in gonadal tissue of patients with ovotesticular syndrome and gonadal dysgenesis 46,XY and 46,XX

F. Suárez, Camila Céspedes, Catalina Forero, 2021, Revista Mexicana de Urología.