Lacrimo‐auriculo‐dento‐digital syndrome: A novel mutation in a Korean family and review of literature-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Lacrimo‐auriculo‐dento‐digital syndrome: A novel mutation in a Korean family and review of literature

Published:2020-07-26 Issue:10 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Ryu Young Hye¹^ORCID,Kyun Chae Jong²,Kim Jung‐Wook²³^ORCID,Lee Soyoung¹^ORCID

Affiliation:

1. Department of Pediatrics Seoul National University Children's HospitalSeoul National University College of Medicine Seoul Korea

2. Department of Pediatric Dentistry School of Dentistry & Dental Research Institute Seoul National University Seoul Korea

3. Department of Molecular Genetics School of Dentistry & Dental Research Institute Seoul National University Seoul Korea

Funder

Korean Government National Research Foundation of Korea

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1412

Reference31 articles.

1. Epiglottic Hypoplasia Associated with Lacrimo-Auriculo-Dental-Digital Syndrome

2. Orodental findings of a family with lacrimo-auriculo-dento digital (LADD) syndrome

3. Dental issues in lacrimo-auriculo-dento-digital syndrome

4. CT findings of head and neck anomalies in lacrimo-auriculo-dento-digital (LADD) syndrome

5. The lacrimo-auriculo-dento-digital syndrome

Cited by 13 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. Ectopic Activation of Fgf8 in Dental Mesenchyme Causes Incisor Agenesis and Molar Microdontia;International Journal of Molecular Sciences;2024-06-27

2. Deciphering the etiology of undiagnosed ocular anomalies along with systemic alterations in pediatric patients through whole exome sequencing;Scientific Reports;2024-06-22

3. Variants in FGF10 cause early onset of severe childhood interstitial lung disease: A detailed description of four affected children;Pediatric Pulmonology;2023-08-10

4. A neglected case of major salivary gland aplasia causing multi-surface caries and periapical radiolucencies: Review of literature and case report;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2023-08

5. Craniofacial anomalies in a murine model of heterozygous fibroblast growth factor 10 gene mutation;Orthodontics & Craniofacial Research;2023-07-14

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