Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics,Molecular Biology
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1. Lhx4 surpasses its paralog Lhx3 in promoting the differentiation of spinal V2a interneurons;Cellular and Molecular Life Sciences;2024-07-06
2. Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes;ARCH ENDOCRIN METAB;2024
3. Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes;Archives of Endocrinology and Metabolism;2023-11-13
4. Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report;World Journal of Clinical Cases;2022-11-06
5. Copy Number Variants Contributing to Combined Pituitary Hormone Deficiency;International Journal of Molecular Sciences;2020-08-11
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