11th Biennial International 22q11.2 Conference

第11届双年度国际22q11.2会议

• 批准号: 383683
• 负责人: Bassett Anne S
• 金额: $ 1.46万
• 依托单位: Centre for Addiction and Mental Health (Toronto)
• 依托单位国家: 加拿大
• 项目类别: Miscellaneous Programs
• 财政年份: 2018
• 资助国家: 加拿大
• 起止时间: 2018-03-01 至 2019-03-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=383683&lang=en
• 关键词: 22q11.2 Deletion Syndrome; Genetic Syndrome; Genetics; Genomic Disorders

About 1 in 3,000 babies are born with a missing piece of DNA on chromosome 22. This condition is called "22q11.2 deletion syndrome" (abbreviated here as "22q"). Babies born with 22q have a high risk of having birth defects, learning difficulties, and othe

大约每3,000个婴儿中就有一个在22号染色体上缺失了DNA。这种情况被称为“22q11.2缺失综合征”（简称为“22 q”）。出生时有22 q的婴儿有很高的出生缺陷、学习困难等风险。