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HESX1 gene

Discuss publications and research concerning the HESX1 gene.

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Related literature

Pituitary Hypoplasia.
HESX1
Pituitary Stalk Interruption Syndrome: From Clinical Findings to Pathogenesis.
HESX1
Classical and non-classical causes of GH deficiency in the paediatric age.
HESX1
Genetic causes of isolated and combined pituitary hormone deficiency.
HESX1
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.
HESX1
A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes.
HESX1
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
HESX1
Pituitary development: a complex, temporal regulated process dependent on specific transcriptional factors.
HESX1
Phenotype-genotype correlations in congenital isolated growth hormone deficiency (IGHD).
HESX1
[Genetic aspects of growth hormone deficiency].
HESX1

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