Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndrome

Published:2011-10 Issue:4 Volume:20 Page:187-189
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Cosar Hese,Kahramaner Zelal,Erdemir Aydin,Turkoglu Ebru,Kanik Ali,Sutcuoglu Sumer,Onay Hüseyin,Alpman Asude,Ozkinay Ferda,Ozer Esra Arun

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Cited by 8 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. Clinical and molecular genetic findings of Crisponi/cold‐induced sweating syndrome (CS/CISS) spectrum in patients from Turkey;Clinical Genetics;2022-07-12

2. Crisponi/cold‐induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts;Clinical Genetics;2019-09-16

3. A case report of Crisponi/cold-induced sweating syndrome 1 in a Saudi family;Journal of Clinical Neonatology;2018

4. A new case series of Crisponi syndrome in a Turkish family and review of the literature;Clinical Dysmorphology;2017-04

5. Congenital Trismus From Brainstem Dysgenesis: Case Report and Review of Literature;Pediatrics;2016-07-01

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