Angelman syndrome
Australian Researchers Adapt Melt Curve Methylation Test for Infant Rare Genetic Disorder Screening
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The test combines melt curve analysis and high-throughput, quantitative PCR to detect Prader-Willi, Angelman, and Dup15q syndromes in infants.
DNA Methylation Mapping in Genetic Syndromes Leads to Disease-Specific Episignatures
Researchers identified 34 episignatures that could be used for diagnostic testing and the interpretation of ambiguous genetic test results.
Ovid Therapeutics, NeuroPointDX Form Biomarker Partnership
The companies will work together to identify novel biomarkers of the rare genetic disorder Angelman syndrome.
BioArray Briefs: 2009.03.31
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Baylor College of Medicine, Illumina, Aushon Biosystems, SciGene, Invitrogen
Baylor to Use Illumina's Infinium Products in Developmental Diseases Studies
Baylor will use the arrays for studying genomic imprinting and its role in developmental diseases.
Feb 25, 2009