Associated Papers
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
American Journal of Human Genetics, 2026
Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing.
Ferrasse A et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
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