ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2003.00139.x/fullpdf
Reference20 articles.
1. Classification and identification of inherited brachydactylies;Fitch;J Med Genet,1979
2. Characteristic facies in type B brachydactyly?;Houlston;Clin Dysmorphol,1994
3. Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation;Gong;Am J Hum Genet,1999
4. Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneity;Oldridge;Am J Hum Genet,1999
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. A novel variant in the ROR2 gene underlying brachydactyly type B: a case report;BMC Pediatrics;2022-09-05
2. Interdigital Hyperplasia in Holstein Cattle Is Associated With a Missense Mutation in the Signal Peptide Region of the Tyrosine-Protein Kinase Transmembrane Receptor Gene;Frontiers in Genetics;2019-11-13
3. Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population;Scientific Reports;2018-08-24
4. Wnt signaling in cartilage development and diseases: lessons from animal studies;Laboratory Investigation;2015-12-07
5. A new mutation in the gene ROR2 causes brachydactyly type B1;Gene;2014-08
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