BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder

Author:

Scott Tiana M.1ORCID,Guo Hui23ORCID,Eichler Evan E.24,Rosenfeld Jill A.5ORCID,Pang Kaifang67,Liu Zhandong67,Lalani Seema5,Bi Weimin58ORCID,Yang Yaping5ORCID,Bacino Carlos A.5,Streff Haley5ORCID,Lewis Andrea M.5,Koenig Mary K.9,Thiffault Isabelle1011ORCID,Bellomo Allison12,Everman David B.12ORCID,Jones Julie R.12,Stevenson Roger E.12,Bernier Raphael131415,Gilissen Christian1617ORCID,Pfundt Rolph16,Hiatt Susan M.18ORCID,Cooper Gregory M.18,Holder Jimmy L.67,Scott Daryl A.519ORCID

Affiliation:

1. Brigham Young University Provo Utah

2. Department of Genome SciencesUniversity of Washington School of Medicine Seattle Washington

3. Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Center for Medical GeneticsCentral Southern University Changsha Hunan China

4. Howard Hughes Medical InstituteUniversity of Washington Seattle Washington

5. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas

6. Department of Pediatrics and Developmental NeuroscienceBaylor College of Medicine Houston Texas

7. Jan and Dan Duncan Neurological Research InstituteTexas Children's Hospital Houston Texas

8. Baylor Genetics Houston Texas

9. Department of Pediatrics, McGovern Medical SchoolThe University of Texas Health Sciences Center at Houston Houston Texas

10. University of Missouri‐Kansas City School of Medicine Kansas City Missouri

11. Department of PathologyChildren's Mercy Hospitals and Clinics Kansas City Missouri

12. Greenwood Genetic Center Greenwood South Carolina

13. Department of Psychiatry and Behavioral SciencesUniversity of Washington Seattle Washington

14. Seattle Children's Autism CenterUniversity of Washington Seattle Washington

15. Center on Human Development and DisabilityUniversity of Washington Seattle Washington

16. Department of Human GeneticsRadboud University Medical Center Nijmegen The Netherlands

17. Radboud Institute for Molecular Life SciencesRadboud University Medical Center Nijmegen The Netherlands

18. HudsonAlpha Institute for Biotechnology Huntsville Alabama

19. Department of Molecular Physiology and BiophysicsBaylor College of Medicine Houston Texas

Funder

National Institute of Neurological Disorders and Stroke

National Human Genome Research Institute

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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