Dominant omodysplasia—A sporadic case—A new case report and review of the literature-Reference-Cited by-同舟云学术

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Dominant omodysplasia—A sporadic case—A new case report and review of the literature

Published:2022-08 Issue:8 Volume:10 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Arabzadeh Aidin¹,Baghianimoghadam Behnam¹^ORCID,Nabian Mohammad Hossein²,Fallah Yousef³,Ebrahimnasab Mohammad Mehdi¹

Affiliation:

1. Department of Orthopedic Surgery Tehran University of Medical Sciences, Imam Khomeini Hospital Complex Tehran Iran

2. Department of Orthopedic Surgery, Shariati Hospital Tehran University of Medical Sciences Tehran Iran

3. Department of Orthopedic Surgery, Sina Hospital Tehran University of Medical Sciences Tehran Iran

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.6187

Reference14 articles.

1. Omodysplasia

2. Omodysplasia: An affected mother and son

3. Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia

4. A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia

Cited by 1 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. FZD2 regulates limb development by mediating β-catenin-dependent and -independent Wnt signaling pathways;Disease Models & Mechanisms;2023-03-01

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