![Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause - ScienceDirect Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2213671119303753-gr4.jpg)
Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause - ScienceDirect
![Characterization of a novel HESX1 mutation in a pediatric case of septo‐optic dysplasia - Pozzi - 2017 - Clinical Case Reports - Wiley Online Library Characterization of a novel HESX1 mutation in a pediatric case of septo‐optic dysplasia - Pozzi - 2017 - Clinical Case Reports - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8ff6ae43-a6f8-480c-8ab6-35881340a475/ccr3868-fig-0001-m.jpg)
Characterization of a novel HESX1 mutation in a pediatric case of septo‐optic dysplasia - Pozzi - 2017 - Clinical Case Reports - Wiley Online Library
![JCI - A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction JCI - A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction](https://dm5migu4zj3pb.cloudfront.net/manuscripts/18000/18589/medium/JCI0318589.f4.jpg)
JCI - A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction
![Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2F477/MediaObjects/41588_1998_BFng0698_125_Fig3_HTML.jpg)
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics
![Novel mutations associated with combined pituitary hormone deficiency in: Journal of Molecular Endocrinology Volume 46 Issue 3 (2011) Novel mutations associated with combined pituitary hormone deficiency in: Journal of Molecular Endocrinology Volume 46 Issue 3 (2011)](https://jme.bioscientifica.com/view/journals/jme/46/3/images/large/R93fig2.jpeg)
Novel mutations associated with combined pituitary hormone deficiency in: Journal of Molecular Endocrinology Volume 46 Issue 3 (2011)
![Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2F477/MediaObjects/41588_1998_BFng0698_125_Fig1_HTML.jpg)
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse | Nature Genetics
![Model of mutant HESX1 effects on the PROP1-dependent program during... | Download Scientific Diagram Model of mutant HESX1 effects on the PROP1-dependent program during... | Download Scientific Diagram](https://www.researchgate.net/publication/5462007/figure/fig1/AS:339596492722189@1457977522081/Model-of-mutant-HESX1-effects-on-the-PROP1-dependent-program-during-pituitary.png)