Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing

por Velasco, Harvy Mauricio, Morales, Jessica L
Publicado no Appl Clin Genet (2017)

SHOX gene and conserved noncoding element deletions/duplications in Colombian patients with idiopathic short stature

por Sandoval, Gloria Tatiana Vinasco, Jaimes, Giovanna Carola, Barrios, Mauricio Coll, Cespedes, Camila, Velasco, Harvy Mauricio
Publicado em 2014