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    P478: Genetic insights into Snijders Blok-Campeau Syndrome: A case study of a homozygous CHD3 variant and comorbidities

    P478: Genetic insights into Snijders Blok-Campeau Syndrome: A case study of a homozygous CHD3 variant and comorbidities by Megan Harrison, Shane Reeves, Robert Conway, Christina Sloan-Heggen

    Published 2025-01-01
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