Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2

Author:

Zarate Yuri A.1ORCID,Bosanko Katherine A.1,Thomas Mary Ann2,Miller David T.3,Cusmano‐Ozog Kristina4,Martinez‐Monseny Antonio5ORCID,Curry Cynthia J.6,Graham John M.7,Velsher Lea8,Bekheirnia Mir Reza9,Seidel Veronica10,Dedousis Demitrios11,Mitchell Anna L.11,DiMarino Amy M.12,Riess Angelika13,Balasubramanian Meena14ORCID,Fish Jennifer L.15,Caffrey Aisling R.16,Fleischer Nicole17,Pierson Tyler Mark18,Lacro Ronald V.19

Affiliation:

1. Section of Genetics and Metabolism University of Arkansas for Medical Sciences Little Rock Arkansas USA

2. Departments of Medical Genetics and Pediatrics Cumming School of Medicine, University of Calgary Calgary Alberta Canada

3. Division of Genetics and Genomics Boston Children's Hospital Boston Massachusetts USA

4. Department of Pathology Stanford University Medical Center Stanford California USA

5. Department of Clinical Genetics and Rare Disease Paediatric Unit Hospital Sant Joan de Déu, University of Barcelona Barcelona Spain

6. Genetic Medicine, Department of Pediatrics University of California, San Francisco/Fresno Fresno California USA

7. Medical Genetics, Department of Pediatrics Cedars‐Sinai Medical Center Los Angeles California USA

8. Genetics Division North York General Toronto Ontario Canada

9. Departments of Pediatrics and Molecular and Human Genetics Baylor College of Medicine Houston Texas USA

10. Clinical Genetics, Department of Pediatrics HGU Gregorio Marañón Madrid Spain

11. Department of Genetics and Genome Sciences University Hospitals Center for Human Genetics Cleveland Ohio USA

12. Division of Pediatric Pulmonology UH Rainbow Babies and Children's Hospital Cleveland Ohio USA

13. Institute of Medical Genetics and Applied Genomics, Medical faculty, University of Tuebingen Tuebingen Germany

14. Sheffield Clinical Genetics Service Sheffield Children's NHS Foundation Trust Sheffield UK

15. Department of Biological Sciences University of Massachusetts Lowell Lowell Massachusetts United States

16. Health Outcomes, College of Pharmacy University of Rhode Island Kingston Rhode Island USA

17. FDNA Inc Boston Massachusetts USA

18. Departments of Pediatrics and Neurology The Board of Governors Regenerative Medicine Institute, Cedars Sinai Medical Center Los Angeles California USA

19. Department of Cardiology, Boston Children's Hospital and Department of Pediatrics Harvard Medical School Boston Massachusetts USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 13 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

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