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
| Image |  |
|---|---|
| Description | scientific article |
| Author/s |
author: Anita Hokken-Koelega André Uitterlinden Jesús Argente |
| Publication date | April 14, 2010 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |