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

Laura de Graaff, J Argente, Danielle Veenma, M Drent, André Uitterlinden, Anita Hokken - Koelega

Research output: Contribution to journalArticleAcademicpeer-review

30 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)363-371
Number of pages9
JournalHormone Research
Publication statusPublished - 2010

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