Detecting congenital hypothyroidism with newborn screening: the relevance of thyroid-stimulating hormone cutoff values Stela Maris Silvestrin, Claudio Leone, Cléa Rodrigues Leone

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

Genomic imbalances in syndromic congenital heart disease Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Josiane Souza, Agnes Cristina Fett-Conte, Têmis Maria Félix, Isabella Lopes Monlléo, Vera Lúcia Gil-da-Silva-Lopes