Complete COL1A1 allele deletions in osteogenesis imperfecta-Reference-Cited by-同舟云学术

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Complete COL1A1 allele deletions in osteogenesis imperfecta

Published:2010-11 Issue:11 Volume:12 Page:736-741
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

van Dijk Fleur S.,Huizer Margriet,Kariminejad Ariana,Marcelis Carlo L.,Plomp Astrid S.,Terhal Paulien A.,Meijers-Heijboer Hanne,Weiss Marjan M.,van Rijn Rick R.,Cobben Jan M.,Pals Gerard

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference30 articles.

Cited by 33 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. Analysis of miRNAs in Osteogenesis imperfecta Caused by Mutations in COL1A1 and COL1A2: Insights into Molecular Mechanisms and Potential Therapeutic Targets;Pharmaceuticals;2023-10-04

2. Normal Variants, Congenital, and Acquired Disorders;Forensic Aspects of Paediatric Fractures;2023

3. Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants;Bone;2022-02

4. Understanding the genetics of intracranial aneurysms: A primer;Clinical Neurology and Neurosurgery;2022-01

5. Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature;Journal of Pediatric Genetics;2021-11-02

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