Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation

Published:2018-03-25 Issue:4 Volume:176 Page:992-996
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Danyel Magdalena¹,Kortüm Fanny²,Dathe Katarina¹³,Kutsche Kerstin²^ORCID,Horn Denise¹^ORCID

Affiliation:

1. Institut für Medizinische Genetik und HumangenetikCharité – Universitätsmedizin BerlinBerlin Germany

2. Institut für HumangenetikUniversitätsklinikum Hamburg‐EppendorfHamburg Germany

3. Pharmakovigilanz‐ und Beratungszentrum für EmbryonaltoxikologieCharité – Universitätsmedizin BerlinBerlin Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38635

Reference15 articles.

1. Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

2. Murine Dishevelled 3 Functions in Redundant Pathways with Dishevelled 1 and 2 in Normal Cardiac Outflow Tract, Cochlea, and Neural Tube Development

3. PHACE Syndrome

4. Dishevelled Paralogs in Vertebrate Development: Redundant or Distinct?

5. The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway

Cited by 14 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. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease;International Journal of Molecular Sciences;2024-02-01

2. Mesomelic Dwarfism;Prenatal Diagnosis of Fetal Osteopathologies;2024

3. Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway;Current Topics in Developmental Biology;2023

4. Nuclear Dishevelled: An enigmatic role in governing cell fate and Wnt signaling;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2022-10

5. 3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities;Molecular Cytogenetics;2022-03-03

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