A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment
Author:
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. A Case Series of Three Patients with Cleidocranial Dysplasia: Clinical Presentation and Diagnostic Considerations;The Cleft Palate Craniofacial Journal;2024-02-27
2. Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type;Frontiers in Genetics;2022-03-16
3. Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey;American Journal of Medical Genetics Part A;2021-05-13
4. Cleidocranial dysplasia with growth hormone deficiency: a case report;BMC Pediatrics;2020-01-16
5. Identification of RUNX2 variants associated with cleidocranial dysplasia;Hereditas;2019-09-16
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