Mutations Within the Transcription Factor <i>PROP1</i> in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency-Reference-Cited by-同舟云学术

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Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Published:2020-09-01 Issue:3 Volume:12 Page:261-268
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Bulut Fatma Derya^ORCID,Özdemir Dilek Semine^ORCID,Kotan Damla^ORCID,Mengen Eda^ORCID,Gürbüz Fatih^ORCID,Yüksel Bilgin^ORCID

Publisher

Galenos Yayinevi

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 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

2. Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins;Hormones;2023-12-26

3. Long-term follow-up data of patients with Multiple Pituitary Hormone Deficiency;Andes Pediatrica;2023-12-21

4. 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

5. Presentation and diagnosis of childhood-onset combined pituitary hormone deficiency: A single center experience from over 30 years;eClinicalMedicine;2022-09

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