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Inside Precision Medicine Research Supports Use of Genome Sequencing to Diagnose Repeat Expansion Disorder

Chromosome disorders

Man and DNA
News & Features

Research Supports Use of Genome Sequencing to Diagnose Repeat Expansion Disorder

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3D Rendered Illustration, scientific visualisation of a Chromosome
News & Features

Ovid and Healx Enter Partnership to Develop Fragile X Treatment

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3D Rendered Illustration, scientific visualisation of a Chromosome
News & Features

Fragile X and SHANK3 Deletion Syndrome Identified by Walking Patterns

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X and Y chromosomes. Genetics concept. 3D rendered illustration.
News & Features

Fragile X Treatment Shows Promise in Phase II Trial

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Alzheimer's disease: illustration of the amyloid-beta 40 peptide (and others) accumulating to form amyloid fibrils that build up dense amyloid plaques.
News & Features

People With Down’s Syndrome At Risk of Early Alzheimer’s Disease

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Blue jeans denim ribbon (isolated with clipping path) on helping hand support and aged wood for genetic disorder awareness and children's rare disease illness
News & Features

Researchers Move One Step Further Towards Fragile X Syndrome Treatment

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Rotating DNA, Genetic engineering scientific concept, blue tint. 3d rendering
Molecular Dx

Genome’s Dark Matter Illuminated by CRISPR, Nanopore Sequencing

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ArcherDx has expanded further into assay development with its acquisition of Baby Genes. Through the purchase
Molecular Dx

ArcherDx Expands Further into Assay Development by Acquiring Baby Genes

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Childhood Education
Molecular Dx

New Pharmacological Approaches May Mitigate Some Fragile X Symptoms

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Source: CDC
Molecular Dx

A Simple and Cheap Molecular Diagnostic for Fragile X-Disorders

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