Hyaline fibromatosis syndrome with a novel 4.41‐kb deletion in <i>ANTXR2</i> gene: A case report and literature review-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Hyaline fibromatosis syndrome with a novel 4.41‐kb deletion in ANTXR2 gene: A case report and literature review

Published:2022-06-20 Issue:8 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Zhu Yunqian¹,Du Xiaonan²,Sun Li³,Wang Huijun⁴^ORCID,Wang Dahui⁵,Wu Bingbing⁴^ORCID

Affiliation:

1. Department of Neonatology Children's Hospital of Fudan University Shanghai China

2. Department of Neurology Children's Hospital of Fudan University Shanghai China

3. Department of Rheumatism Children's Hospital of Fudan University Shanghai China

4. Clinical Genetic Center Children's Hospital of Fudan University Shanghai China

5. Department of Orthopedics Children's Hospital of Fudan University Shanghai China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1993

Reference20 articles.

1. Differential gene expression during capillary morphogenesis in 3D collagen matrices

2. Juvenile hyaline fibromatosis: a case report follow-up after 3 years and a review of the literature

3. Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations

4. Novel variation in ANTXR2 gene causing hyaline fibromatosis syndrome: A report from India

5. Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system

Cited by 10 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. Hyaline Fibromatosis Syndrome Diagnosed by Whole Genome Sequencing;Journal of Pediatric Health Care;2024-09

2. Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome;The Turkish Journal of Pediatrics;2024-05-23

3. Investigating the Influence of ANTXR2 Gene Mutations on Protective Antigen Binding for Heightened Anthrax Resistance;Genes;2024-03-28

4. Prognostic factors for wellbeing in patients with hyaline fibromatosis syndrome;Pediatrics International;2024-01

5. Identification and verification of genes associated with hypoxia microenvironment in Alzheimer’s disease;Scientific Reports;2023-09-27

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3