Identification and molecular characterization of two novel chromosomal deletions associated with autism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01395.x/fullpdf
Reference32 articles.
1. Epidemiological surveys of autism and other pervasive developmental disorders: an update;Fombonne;J Autism Dev Disord,2003
2. Pervasive developmental disorders in preschool children: confirmation of high prevalence;Chakrabarti;Am J Psychiatry,2005
3. Genetics of autism: complex aetiology for a heterogeneous disorder;Folstein;Nat Rev Genet,2001
4. Molecular genetics of autism spectrum disorder;Veenstra-VanderWeele;Mol Psychiatry,2004
5. Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder;Reddy;BMC Med Genet,2005
Cited by 54 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. Chromosomal aberration detection in Iraqi children with autism;Human Gene;2023-12
2. Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2023-01
3. SAPAP Scaffold Proteins: From Synaptic Function to Neuropsychiatric Disorders;Cells;2022-11-28
4. Altered synaptic protein expression, aberrant spine morphology, and impaired spatial memory in Dlgap2 mutant mice, a genetic model of autism spectrum disorder;Cerebral Cortex;2022-09-28
5. De novo 4q35.2 duplication containing FAT1 is associated with autism spectrum disorder;Clinical Genetics;2022-07-31
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