Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1

Published:2010-04-13 Issue:6 Volume:31 Page:E1461-E1471
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Richards Allan J.,McNinch Annie,Martin Howard,Oakhill Kim,Rai Harjeet,Waller Sarah,Treacy Becky,Whittaker Joanne,Meredith Sarah,Poulson Arabella,Snead Martin P.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 114 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. Clinician Awareness of Stickler Syndromes Among Australian Allied Health Care Professionals;Journal of Multidisciplinary Healthcare;2024-04

2. The molecular complexity of COL2A1 splicing variants and their significance in phenotype severity;Bone;2024-04

3. Nonperfusion of the Far Peripheral Retina in Highly Myopic Stickler Syndrome;Journal of VitreoRetinal Diseases;2024-03-13

4. Outcomes of rhegmatogenous retinal detachment surgery in patients with Stickler syndrome;Graefe's Archive for Clinical and Experimental Ophthalmology;2024-02-15

5. Exome sequencing‐aided precise diagnosis of four families with type I Stickler syndrome;Molecular Genetics & Genomic Medicine;2023-12-11

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