Prevalence of CGG expansions of the FMR1 gene in a US population-based sample-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prevalence of CGG expansions of the FMR1 gene in a US population-based sample

Published:2012-05-22 Issue:5 Volume:159B Page:589-597
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Seltzer Marsha Mailick,Baker Mei Wang,Hong Jinkuk,Maenner Matthew,Greenberg Jan,Mandel Daniel

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.32065/fullpdf

Reference44 articles.

1. Co-occurring conditions associated with FMR1 gene variations: Findings from a National Parent Survey;Bailey;Am J Med Genet Part A,2008

2. Preconceptional and prenatal screening for fragile X syndrome: Experience with 40,000 tests;Berkenstadt;Prenat Diagn,2007

3. Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation;Berry-Kravis;Ann Neurol,2004

4. Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers;Bourgeois;J Clin Genet,2011

5. FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure;Bretherick;Human Genet,2005

Cited by 165 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. Intrasubject variability of sustained attention is associated with elevated self-reported attention deficits in women with a fragile X premutation allele.;Neuropsychology;2024-09

2. Social Communication Delay in an Unbiased Sample of Preschoolers With the FMR1 Premutation;Journal of Speech, Language, and Hearing Research;2024-07-09

3. Strategic Implementation of Fragile X Carrier Screening in China;The Journal of Molecular Diagnostics;2024-07

4. A Comprehensive Review of Fragile X Syndrome and Fragile X Premutation Associated Conditions in Africa;Genes;2024-05-25

5. Autistic Traits Associated with the Fragile X Premutation Allele: The Neurodevelopmental Profile;Developmental Neuropsychology;2024-05-16

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

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