Enabling Genomic Medicine 2021

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Rare disease as a jigsaw - Timothy Syndrome

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Expanding our understanding of skeletal dysplasia

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Ensuring parents have a voice in their child’s care

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The long road to diagnosis: Pitt-Hopkins Syndrome

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Congenica is Joint Winner of MIT Solve The Horizon Prize

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Congenica announced as a finalist for MIT Solve’s Horizon Prize

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Accelerating NGS analysis at ESHG 2021

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Automating Clinical Genomic Analysis & Reporting for Rapid NGS Results

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Congenica signs distribution agreement with ATC Healthcare in Turkey

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Living with a rare disease in perspective: Lynsey’s Rare Journey

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Enabling Genomic Medicine 2021

Read More

Rare disease as a jigsaw - Timothy Syndrome

Read More

Expanding our understanding of skeletal dysplasia

Read More

Ensuring parents have a voice in their child’s care

Read More

The long road to diagnosis: Pitt-Hopkins Syndrome

Read More

Congenica is Joint Winner of MIT Solve The Horizon Prize

Read More

Congenica announced as a finalist for MIT Solve’s Horizon Prize

Read More

Accelerating NGS analysis at ESHG 2021

Read More

Automating Clinical Genomic Analysis & Reporting for Rapid NGS Results

Read More

Congenica signs distribution agreement with ATC Healthcare in Turkey

Read More

Living with a rare disease in perspective: Lynsey’s Rare Journey

Read More