Expanding the phenotypic profile of Kleefstra syndrome: A female with low-average intelligence and childhood apraxia of speech

Author:

Samango-Sprouse Carole1234,Lawson Patrick2,Sprouse Courtney5,Stapleton Emily2,Sadeghin Teresa12,Gropman Andrea56

Affiliation:

1. Neurodevelopmental Diagnostic Center for Young Children; Crofton Maryland

2. The Focus Foundation; Davidsonville Maryland

3. Department of Pediatrics; George Washington University; Washington District of Columbia

4. Department of Human and Molecular Genetics; Florida International University; Miami Florida

5. Department of Neurology; Children's National Medical Center; Washington District of Columbia

6. George Washington University of the Health Sciences; Washington District of Columbia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference14 articles.

1. Developmental coordination disorder: What is it;Dewey;Phys Occup Ther Pediatr,2001

2. Language growth in children with expressive language delay;Fischel;Pediatrics,1989

3. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype;Kleefstra;J Med Genet,2009

4. Kleefstra syndrome;Kleefstra;Gene Rev,1993

5. The efficacy of treatment for children with developmental speech and language delay/disorder: A meta-analysis;Law;J Speech Lang Hear Res,2004

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