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机译:A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype
Department of Child, Women, General and Specialized Surgery,University of Campania;
University of Trieste;
Institute for Maternal and Child Health IRCCS Burlo GarofoloPediatric Endocrine Unit,IRCCS Azienda Ospedaliero-Universitaria Di BolognaPediatric Endocrine Unit, Department of Translational Medical Sciences,University Federico IIDepartment of Pediatrics,IRCCS Istituto Giannina GasliniDepartment of Biomedical Sciences and Human Oncology, Pediatric Unit,University of Bari A. MoroEndocrinology Unit,University-Hospital Pediatric Department, Bambino Gesù Children’s Hospital, IRCSSUnit of Paediatrics, Department of Human Pathology of Adulthood and Childhood,University of MessinaUnit of Pediatrics, Department of Maternal and Child Health,Carlo Poma Hospital, ASST-MantovaPediatric Unit-“M. Bufalini” Hospital - Cesena;
DLK1; Mutations; Precocious puberty; molecular screening; Genetics;