A c.1019A > G mutation inFGFR2, which predicts p.Tyr340Cys, in a lethally malformed fetus with Pfeiffer syndrome and multiple pterygia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference19 articles.
1. American Journal of Medical Genetics 01487299 10968628 2004
2. Cutis gyratum, acanthosis nigricans and other congenital anomalies. A new syndrome;Beare;Br J Dermatol,1969
3. Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome;Cornejo-Roldan;Hum Genet,1999
4. A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis;Eswarakumar;Proc Natl Acad Sci USA,2004
5. Arthrogryposis multiplex congenita: Etiology, genetics, classification, diagnostic approach, and general aspects;Hall;J Pediatr Orthop B,1997
Cited by 7 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. Perinatal imaging findings of a fetus with Pfeiffer syndrome and a heterozygous c.1019A>G, p.Tyr340Cys (Y340C) mutation in FGFR2 presenting a cloverleaf skull, craniosynostosis and short limbs on prenatal ultrasound mimicking thanatophoric dysplasia type II;Taiwanese Journal of Obstetrics and Gynecology;2024-05
2. Pena-Shokeir syndrome: current management strategies and palliative care;The Application of Clinical Genetics;2018-10
3. Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis;The Journal of Maternal-Fetal & Neonatal Medicine;2016-10-20
4. Arthrogryposes (Multiple Congenital Contractures);Emery and Rimoin's Principles and Practice of Medical Genetics;2013
5. Arthrogryposis and fetal hypomobility syndrome;Handbook of Clinical Neurology;2013
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