RARE Bears bring community together on Rare Disease Day

Read More

Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders

Read More

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

Read More

A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder

Read More

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Read More

Congenica named MedTech Company of the Year 2019

Read More

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

Read More

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Read More

Congenica brings together Mastermind, DECIPHER and Sentieon in major product update

Read More

Congenica Integrates Powerful New Curated Data

Read More

Highlights from the International Conference on Prenatal Diagnosis and Therapy

Read More

RARE Bears bring community together on Rare Disease Day

Read More

Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders

Read More

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

Read More

A fast and reliable method to reach a conclusive diagnosis of MYH9-related disorder

Read More

Congenica Appoints Dr. Heiner Dreismann as Non-Executive Director

Read More

Congenica named MedTech Company of the Year 2019

Read More

ExomeCG to simplify molecular and cytogenomic data generation and interpretation

Read More

Prenatal exome sequencing in unexplained fetal oedema: a game changer

Read More

Congenica brings together Mastermind, DECIPHER and Sentieon in major product update

Read More

Congenica Integrates Powerful New Curated Data

Read More

Highlights from the International Conference on Prenatal Diagnosis and Therapy

Read More