<i>PROP1, HESX1, POU1F1, LHX3 </i>and<i> LHX4</i> Mutation and Deletion Screening and <i>GH1 </i>P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency | Publicación