Evaluation of Clinical Utility and Cost-effectiveness of Genome-Wide Sequencing in the Canadian Rare Genetic Disease Clinic
Evaluation of Clinical Utility and Cost-effectiveness of Genome-Wide Sequencing in the Canadian Rare Genetic Disease Clinic
加拿大罕见遗传病诊所全基因组测序的临床实用性和成本效益评估
批准号：
365414
负责人：
Hartley Taila S
金额：
$7.65万
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2016
资助国家：
加拿大
项目状态：
已结题
起止时间：
2016-10-01 至 2019-10-01
中文摘要
翻译
罕见疾病影响多达十二分之一的加拿大人。这些人中的许多人经历了诊断的奥德赛;他们由多名医疗专业人员进行评估，但缺乏准确的诊断和治疗计划。罕见疾病通常由以下原因引起：
英文摘要
Rare diseases affect as many as one in twelve Canadians. Many of these individuals experience a diagnostic odyssey; they are evaluated by multiple medical professionals, but lack an accurate diagnosis and treatment plan. Rare diseases are often caused by
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
海外基金
