Towards adequate national provision of genomic testing in pregnancy
Towards adequate national provision of genomic testing in pregnancy
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
中文摘要
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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.
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Novel Fragile X Syndrome prevalence estimates in 100,000 Australian newborns, prognostic and health-economic outcomes: a retrospective newborn screening study
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批准号:nhmrc : GNT1103389
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项目类别:Project Grants
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资助金额:$76.99万
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财政年份:2016
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负责人:A/Pr Howard Slater
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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
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项目类别:Project Grants
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财政年份:2016
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负责人:A/Pr Howard Slater
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依托单位:
Characterization of a novel epigenetic boundary and long range epigenetic modifications specific to FMR1 expansion carriers with behavioural and cognitive disorders - implications for earlier diagnosis and treatment.
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批准号:nhmrc : 1049299
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项目类别:Project Grants
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资助金额:$44.73万
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财政年份:2013
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负责人:A/Pr Howard Slater
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依托单位:
Implementation of a new, inexpensive and high-throughput Matrix Assisted Laser Desorption / Ionization _ Time Of Flight Mass Spectrometry test for superior detection of Fragile X Syndrome in targeted diagnostics and newborn population screening.
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批准号:nhmrc : 1017263
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项目类别:NHMRC Development Grants
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资助金额:$16.95万
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财政年份:2011
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负责人:A/Pr Howard Slater
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依托单位:
海外基金