Associated Papers
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Schmidt A et al.
Nature Genetics, 2024
39039281 (PubMed )
Supplement: 41588_2024_1836_MOESM4_ESM.xlsx › S1
Neurodevelopmental disorders and anti-epileptic treatment in a patient with a SATB1 mutation: A case report.
Yu Y et al.
Frontiers in Pediatrics, 2022
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