Prop1, Hesx1, Pou1F1, Lhx3 and Lhx4 Mutation and Deletion Screening and Gh1 P89l and Ivs3+1/+2 Mutation Screening in A Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency

L.C.G. Graaff, J. Argente, D.C.M. Veenma, M.L. Drent, A.G. Uitterlinden, A.C.S. Hokken-Koelega

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)363-371
JournalHormone Research in Paediatrics
Issue number5
Publication statusPublished - 2010

Cite this