Meier-Gorlin syndrome: an additional case report in an adult woman-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Meier-Gorlin syndrome: an additional case report in an adult woman

Published:2019-04 Issue:2 Volume:28 Page:86-90
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Belaid Rym,Zouaoui Hsan,Yazidi Meriem,Oueslati Ibtissem,Grira Wafa,Chaker Fatma,Chihaoui Melika

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

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

Reference15 articles.

1. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome;Bicknell;Nat Genet,2011

2. Meier-Gorlin syndrome genotype–phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis;De Munnik;Eur J Hum Genet,2012

3. Meier-Gorlin syndrome;De Munnik;Orphanet J Rare Dis,2015

4. Meier-Gorlin syndrome: the adult phenotype;Fryns;Clin Dysmorphol,1998

5. Malformation syndromes. A selected miscellany;Gorlin;Birth Defects Orig Artic Ser,1975

Cited by 1 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. Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation;BMC Pregnancy and Childbirth;2021-05-17

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