Human laterality disorders
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference85 articles.
1. A human syndrome caused by immotile cilia;Afzelius;Science,1976
2. Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome;Ansley;Nature,2003
3. Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left–right laterality defects;Bamford;Nat. Genet.,2000
4. Conjoined twins: prenatal diagnosis and assessment of associated malformations;Barth;Radiology,1990
5. Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia;Bartoloni;Proc. Natl. Acad. Sci. USA,2002
Cited by 126 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. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024
2. Situs inversus totalis in an asymptomatic adolescent - importance of patient education: A case report;World Journal of Clinical Pediatrics;2023-12-09
3. Situs inversus with levocardia in a 15-year-old male adolescent: a case report;Journal of Medical Case Reports;2023-12-03
4. Laparoscopic Living Donor Nephrectomy in a Donor With Situs Inversus Totalis: It is Not a Contraindication to Kidney Transplant;Transplantation Proceedings;2023-10
5. Identification of novel compound heterozygous variants in the DNAH1 gene of a Chinese family with left-right asymmetry disorder;Frontiers in Molecular Biosciences;2023-06-29
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