Clinical, Biochemical and Molecular Investigations of Three Taiwanese Children with Laron Syndrome
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2004.17.2.165/pdf
Reference6 articles.
1. Classification of growth hormone insensitivity syndrome
Cited by 8 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. Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report;BMC Endocrine Disorders;2023-07-20
2. Growth Hormone Receptor Mutations Related to Individual Dwarfism;International Journal of Molecular Sciences;2018-05-10
3. DIAGNOSIS OF ENDOCRINE DISEASE: Limitations of the IGF1 generation test in children with short stature;European Journal of Endocrinology;2012-03
4. Evidence for a Continuum of Genetic, Phenotypic, and Biochemical Abnormalities in Children with Growth Hormone Insensitivity;Endocrine Reviews;2011-04-27
5. Laryngeal and vocal evaluation in untreated growth hormone deficient adults;Otolaryngology–Head and Neck Surgery;2009-01
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