Fibular aplasia, tibial campomelia, and oligosyndactyly in a male newborn infant: A case report and review of the literature
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Congenital deficiency of the fibula
2. Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation
3. Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity
4. Congenital bowing of the long bones
5. Limb deficiency syndrome in half-sibs
Cited by 36 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 Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature;Cureus;2024-07-22
2. A perspective on psychedelic teratogenicity: the utility of zebrafish models;Trends in Pharmacological Sciences;2023-10
3. New pathogenic variant in DLX5: New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly;Frontiers in Genetics;2023-04-13
4. Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome;American Journal of Medical Genetics Part A;2023-01-06
5. A case report on Fibular Aplasia, Tibial Campomelia, Oligosyndactyly Syndrome variant in a Male Infant;Journal of the Pakistan Medical Association;2022-05-10
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