Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus

by Keselman,Ana, Scaglia,Paula A., Rodríguez Prieto,María Soledad, Ballerini,María Gabriela, Rodríguez,María Eugenia, Ropelato,María Gabriela, Bergadá,Ignacio, Jasper,Héctor G., Domené,Horacio M.
Published 2012