The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

Overview of attention for article published in Human Mutation, February 2022

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Open Access UCL Research: The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases https://t.co/263Sof0Kzv

RD-Connect GPAP is an online system that facilitates collation, sharing, analysis and interpretation of genome-phenome datasets for Rare Disease diagnosis and gene discovery - for more information see: https://t.co/3XVoZWgm4F

Want to know more about how the @ConnectRD platform is accelerating diagnosis, research, and gene discovery #RareDisease patient? 👇 https://t.co/xlbyVjtbu3

RT @cnag_eu: Not to miss ➡️ “The @ConnectRD Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare…

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