课题基金 / 基金详情

Towards adequate national provision of genomic testing in pregnancy

Towards adequate national provision of genomic testing in pregnancy
争取在全国范围内提供充足的妊娠期基因组检测
批准号:
nhmrc : 1059993
负责人:
A/Pr Howard Slater
金额:
$34.37万
依托单位国家:
澳大利亚
项目类别:
Project Grants
财政年份:
2014
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

项目摘要

项目成果

A/Pr Howard Slater的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Genomic information about unborn children can now be provided using chromosomal microarrays which have the potential to revolutionize maternal care in Australia, but are currently only used in high risk pregnancies. Soon all pregnant women, the vast majority who currently have prenatal screening, will be able to access this and other genomic technologies. We will examine the psychological impact of fetal genomic testing and, in doing so, assess the need for service planning, as well as potential legal and policy changes in Australia.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study
  • 批准号:
    nhmrc : GNT1103389
  • 项目类别:
    Project Grants
  • 资助金额:
    $76.99万
  • 财政年份:
    2016
  • 负责人:
    A/Pr Howard Slater
  • 依托单位:
Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study
  • 批准号:
    nhmrc : 1103389
  • 项目类别:
    Project Grants
  • 资助金额:
    $52.79万
  • 财政年份:
    2016
  • 负责人:
    A/Pr Howard Slater
  • 依托单位:
海外基金