Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes-Reference-Cited by-同舟云学术

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Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes

Published:2023-11-13 Issue: Volume:68 Page:
ISSN:2359-3997
Container-title:Archives of Endocrinology and Metabolism
language:en
Short-container-title:

Author:

Kırkgöz Tarık^ORCID,Gürsoy Semra^ORCID,Acar Sezer^ORCID,Nalbantoğlu Özlem^ORCID,Özkaya Beyhan^ORCID,Korkmaz Hüseyin Anıl^ORCID,Hazan Filiz^ORCID,Özkan Behzat^ORCID

Publisher

Archives of Endocrinology and Metabolism

Subject

Endocrinology, Diabetes and Metabolism

Reference29 articles.

1. Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era;Fang;Endocr Rev,2016

2. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes;Davis;Mol Cell Endocrinol,2010

3. Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency;Kandemir;Turk J Pediatr,2012

4. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study;Baş;Endocrine,2015

5. Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency;Bulut;J Clin Res Pediatr Endocrinol,2020

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