Epigenomics studies in Beckwith-Wiedemann syndrome

Beckwith-Wiedemann 综合征的表观基因组学研究

• 批准号: 199064
• 负责人: Vanderhooft Rebecca H
• 金额: $ 1.27万
• 依托单位: Hospital for Sick Children (Toronto)
• 依托单位国家: 加拿大
• 项目类别: Studentship Programs
• 财政年份: 2010
• 资助国家: 加拿大
• 起止时间: 2010-02-01 至 2011-02-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=199064&lang=en
• 关键词: Beckwith-Wiedemann Syndrome; Chromosome 11p15; Dna Methylation; Gene Expression; Imprinting; Multiple Loss Of Methylation (Mlom); Overgrowth Disorder

Beckwith-Wiedemann syndrome (BWS) is a childhood disorder characterized by a variety of symptoms, often including overgrowth, macroglossia (large tongue), abdominal wall defects, enlarged organs and size differences between left and right sides of the bod

贝克维斯·韦德曼综合征（BWS）是一种儿童疾病，其特征是多种症状，通常包括过度生长，大舌（大舌），腹壁缺陷，器官肿大以及身体左侧和尺寸差异