Molecular Defects of the <i>CYP21A2</i> Gene in Greek-Cypriot Patients with Congenital Adrenal Hyperplasia-Reference-Cited by-同舟云学术

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Molecular Defects of the CYP21A2 Gene in Greek-Cypriot Patients with Congenital Adrenal Hyperplasia

Published:2011 Issue:3 Volume:75 Page:180-186
ISSN:1663-2826
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Skordis Nicos,Kyriakou Andreas,Tardy Véronique,Ioannou Yiannis S.,Varvaresou Athanasia,Dracopoulou-Vabouli Maria,Patsalis Philippos C.,Shammas Christos,Neocleous Vassos,Phylactou Leonidas A.

Publisher

S. Karger AG

Subject

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

Cited by 20 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 endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center;Orphanet Journal of Rare Diseases;2024-04-18

2. Compromised Adult Height in Females with Non-Classical Congenital Adrenal Hyperplasia Diagnosed in Childhood;Hormone Research in Paediatrics;2023

3. CYP21A2 mutations in pediatric patients with congenital adrenal hyperplasia in Costa Rica;Molecular Genetics and Metabolism Reports;2021-06

4. Analysis of phenotypes and genotypes in 84 patients with 21-Hydroxylase deficiency in southern China;Steroids;2019-11

5. The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective Analysis;Hormone and Metabolic Research;2019-09

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