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pituitary hormone deficiency, combined
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POU1F1
P-OTX: a PIT-1-interacting homeodomain factor expressed during anterior pituitary gland development
Transcription factors regulating pituitary development
Cellular determination in the anterior pituitary gland: PIT-1 and PROP-1 mutations as causes of human combined pituitary hormone deficiency
PROP1
Mutations in PROP1 cause familial combined pituitary hormone deficiency
LHX3
The nuclear LIM domain interactor NLI mediates homo- and heterodimerization of LIM domain transcription factors
LHX4
Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4
HESX1
Pituitary Stalk Interruption Syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
OTX2
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
Developmental rescue of Drosophila cephalic defects by the human Otx genes
OTX2 homeodomain protein binds a DNA element necessary for interphotoreceptor retinoid binding protein gene expression
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