Thirty-three novel COL1A1 and COL1A2 mutations in patients with osteogenesis imperfecta types I-IV-Reference-Cited by-同舟云学术

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Thirty-three novel COL1A1 and COL1A2 mutations in patients with osteogenesis imperfecta types I-IV

Published:2001 Issue:5 Volume:17 Page:434-434
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Ward L.M.,Lalic L.,Roughley P.J.,Glorieux F.H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 39 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. Associations of collagen type 1 α1 gene polymorphisms and musculoskeletal soft tissue injuries: a meta-analysis with trial sequential analysis;Aging;2024-05-22

2. RNA Sequencing of Urine‐Derived Cells for the Characterization and Diagnosis of Osteogenesis Imperfecta;Journal of Bone and Mineral Research;2023-06-23

3. Osteogenesis imperfecta and other defects of bone development as occasional causes of adult osteoporosis;Marcus and Feldman's Osteoporosis;2021

4. The radiologic diagnosis of skeletal dysplasias: past, present and future;Pediatric Radiology;2020-11

5. Compound phenotype of osteogenesis imperfecta and Ehlers–Danlos syndrome caused by combined mutations in COL1A1 and COL5A1;Bioscience Reports;2019-07

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